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L D Mueller

Publications and source records attributed to L D Mueller.

At least 19 recordsLinked to original sources

Evolution of late-life fecundity in Drosophila melanogaster.

Late-life fecundity has been shown to plateau at late ages in Drosophila analogously to late-life mortality rates. In this study, we test an evolutionary theory of late life based on the declining force of natural selection that can explain the occurrence of these late-life plateaus in Drosophila. We also examine the viability of eggs laid by late-age females and test a population genetic mechanism that may be involved in the evolution of late-life fecundity: antagonistic pleiotropy. Together these experiments demonstrate that (i) fecundity plateaus at late ages, (ii) plateaus evolve according to the age at which the force of natural selection acting on fecundity reaches zero, (iii) eggs laid by females in late life are viable and (iv) antagonistic pleiotropy is involved in the evolution of late-life fecundity. This study further supports the evolutionary theory of late life based on the age-specific force of natural selection.

Aging↗

Ageing and immortality.

The concept of the force of natural selection was developed to explain the evolution of ageing. After ageing, however, comes a period in which mortality rates plateau and some individual organisms could, in theory, live forever. This late-life immortality has no presently agreed upon explanation. Two main theories have been offered. The first is heterogeneity within ageing cohorts, such that only extremely robust individuals survive ageing. This theory can be tested by comparisons of more and less robust cohorts. It can also be tested by fitting survival data to its models. The second theory is that late-life plateaus in mortality reflect the inevitable late-life plateau in the force of natural selection. This theory can be tested by changing the force of natural selection in evolving laboratory populations, particularly the age at which the force plateaus. This area of research has great potential for elucidating the overall structure of life-history evolution, particularly the interrelationship between the three life-history phases of development, ageing and immortality.

Aging↗

Testing the heterogeneity theory of late-life mortality plateaus by using cohorts of Drosophila melanogaster.

Variation among individuals in robustness has been posed as a general explanation for the lack of increase in late-life mortality rates. Here, we test corollaries of this heterogeneity theory. One is that populations that have undergone strong laboratory selection for differentiated stress resistance should show significant differences in their late-life mortality schedules. To test this corollary, we employed 40 410 flies from three groups of Drosophila melanogaster populations that differ substantially in their resistance to starvation. No significant differences between these groups were found for late-life mortality. Another corollary of the heterogeneity theory is that there should be late-life plateaus in stress resistance that coincide with the plateau stage of the mortality curve. In 20 994 flies from six replicate outbred laboratory populations, we measured mortality rates every other day and starvation and desiccation resistance every 7 days. Both male and female starvation and desiccation resistance clearly decreased with time overall. There was no late-life plateau in male desiccation resistance. A late-life plateau in male starvation resistance may exist, however. Together, these two experiments generally constitute evidence against heterogeneity as a major contributor to the phenomenon of late-life mortality plateaus.

Animals↗

Poisson distribution of male mating success in laboratory populations of Drosophila melanogaster.

Variation among males and females in reproductive success is a major determinant of effective population size. Most studies of male mating success in Drosophila, however, have been done under conditions very different from those in typical cultures. We determined the distribution of male mating success in five laboratory populations of D. melanogaster maintained on a 14 d, discrete generation cycle fairly representative of standard Drosophila cultures. Mating success was measured as the number of matings a male could achieve under conditions closely approximating a regular culture vial of these populations. Preliminary studies determined that most mating in these populations occurred within 14 h of the flies attaining sexual maturity. Consequently, individual virgin males were marked with white paint on their thorax, put into vials with varying numbers of unmarked virgin flies of both sexes, and monitored continuously for matings over a period of up to 14 h. At various times during the assay, virgin males and females were added to these vials in proportions simulating the pattern of eclosion in culture vials. The observed variation in the number of matings per male in the five populations was, by and large, consistent with a Poisson distribution, suggesting that male mating success in short-generation-time, discrete-generation laboratory cultures of D. melanogaster may fulfil a fundamental assumption of the Wright-Fisher model of genetic drift in finite populations.

Animals↗

Osmoregulation in Drosophila melanogaster selected for urea tolerance.

Animals may adapt to hyperosmolar environments by either osmoregulating or osmoconforming. Osmoconforming animals generally accumulate organic osmolytes including sugars, amino acids or, in a few cases, urea. In the latter case, they also accumulate 'urea-counteracting' solutes to mitigate the toxic effects of urea. We examined the osmoregulatory adaptation of Drosophila melanogaster larvae selected to live in 300 mmol l(-)(1) urea. Larvae are strong osmoregulators in environments with high NaCl or sucrose levels, but have increased hemolymph osmolarity on urea food. The increase in osmolarity on urea food is smaller in the selected larvae relative to unselected control larvae, and their respective hemolymph urea concentrations can account for the observed increases in total osmolarity. No other hemolymph components appear to act as urea-counteractants. Urea is calculated to be in equilibrium across body compartments in both selected and control larvae, indicating that the selected larvae are not sequestering it to lower their hemolymph osmolarity. The major physiological adaptation to urea does not appear to involve increased tolerance or improved osmoregulation per se, but rather mechanisms (e.g. metabolism, decreased uptake or increased excretion) that reduce overall urea levels and the consequent toxicity.

Adaptation, Physiological↗

Evolutionary theory predicts late-life mortality plateaus.

Most demographic data indicate a roughly exponential increase in adult mortality with age, a phenomenon that has been explained in terms of a decline in the force of natural selection acting on age-specific mortality. Scattered demographic findings suggest the existence of a late-life mortality plateau in both humans and dipteran insects, seemingly at odds with both prior data and evolutionary theory. Extensions to the evolutionary theory of aging are developed which indicate that such late-life mortality plateaus are to be expected when enough late-life data are collected. This expanded theory predicts late-life mortality plateaus, with both antagonistic pleiotropy and mutation accumulation as driving population genetic mechanisms.

Adult↗

Genetics of larval urea tolerance in Drosophila melanogaster.

The genetic control of larval tolerance to urea, a nitrogenous waste-product occurring naturally in crowded Drosophila cultures, was investigated in a set of five laboratory populations of D. melanogaster that had been successfully subjected to selection for increased larval urea tolerance. Larva to adult survivorship and development time at three different levels of urea were assayed on the five selected populations, their five matched controls and a set of 10 F1 hybrid populations derived from reciprocal crosses between pairs of selected and control populations. As expected from the results of previous studies, the selected populations exhibited greater larval tolerance to the toxic effects of urea, relative to their controls. Comparison of the hybrid and parental populations with respect to both survivorship and development time indicated that the genetic control of urea tolerance in the selected populations is largely dominant, and has a significant X-linked component. The data also suggested that females from the selected populations exercise a nongenetic maternal effect on the development time of their progeny, regardless of urea level.

Adaptation, Physiological↗

Population density effects on longevity.

Population density, or the number of adults in an environment relative to the limiting resources, may have important long and short term consequences for the longevity of organisms. In this paper we summarize the way in which crowding may have an immediate impact on longevity, either through the phenomenon known as dietary restriction or through alterations in the quality of the environment brought on by the presence of large numbers of individuals. We also consider the possible long term consequences of population density on longevity by the process of natural selection. There has been much theoretical speculation about the possible impact of population density on the evolution of longevity but little experimental evidence has been gathered to test these ideas. We discuss some of the theory and empirical evidence that exists and show that population density is an important factor in determining both the immediate chances of survival and the course of natural selection.

Animals↗

The effect of superoxide dismutase alleles on aging in Drosophila.

The effects of superoxide dismutase on aging were tested using two different experimental approaches. In the first, replicated populations with postponed aging were compared with their controls for frequencies of electrophoretic alleles at the SOD locus. Populations with postponed aging had consistently greater frequencies of the allele coding for more active SOD protein. This allele was not part of a segregating inversion polymorphism. The second experimental approach was the extraction of SOD alleles from different natural populations followed by the construction of different SOD genotypes on hybrid genetic backgrounds. This procedure did not uncover any statistical effect of SOD genotype on longevity or fecundity. There were large effects on longevity and fecundity due to the family from which a particular SOD genotype was derived. To detect the effects of SOD genotypes on longevity with high probability would require a ten-fold increase in the number of families used.

Aging↗

Genetic variation and random drift in autotetraploid populations.

The rate of decay of genetic variation is determined for randomly mating autotetraploid populations of finite size, and the equilibrium homozygosity under mutation and random drift is calculated. It is shown that heterozygosity is lost at a slower rate than in diploid populations, and that the equilibrium heterozygosity with mutation and random drift is higher than for diploids. Outcrossing populations as well as populations that randomly self are analyzed. A method of comparing genetic variation between autotetraploid and diploid populations is proposed. Our treatment suggests that the "gametic homozygosity" provides a unified approach for comparing genotypes within a population as well as comparing genetic variation between populations with different levels of ploidy.

Alleles↗

Evolution of behavior by density-dependent natural selection.

Theories of density-dependent natural selection predict that evolution should favor those genotypes with the highest per capita rates of population growth under the current density conditions. These theories are silent about the mechanisms that may give rise to these increases in density-dependent growth rates. We have observed the evolution of six populations of Drosophila melanogaster recently placed in crowded environments after nearly 200 generations at low-population density in the laboratory. After 25 generations in these crowded cultures all six populations showed the predicted increase in population growth rates at high-population density with the concomitant decrease in their growth rates at low densities. These changes in rates of population growth are accompanied by changes in the feeding and pupation behavior of the larvae: those populations that have evolved at high-population densities have higher feeding rates and are less likely to pupate on or near the food surface than populations maintained at low densities. These changes in behavior serve to increase the competitive ability of larvae for limited food and reduce mortality under crowded conditions during the pupal stage of development. A detailed understanding of the mechanisms by which populations evolve under density-dependent natural selection will provide a framework for understanding the nature of trade-offs in life history evolution.

Animals↗

Density-dependent natural selection and trade-offs in life history traits.

Theories of density-dependent natural selection state that at extreme population densities evolution produces alternative life histories due to trade-offs. The trade-offs are presumed to arise because those genotypes with highest fitness at high population densities will not also have high fitness at low density and vice-versa. These predictions were tested by taking samples from six populations of Drosophila melanogaster kept at low population densities (r-populations) for nearly 200 generations and placing them in crowded cultures (K-populations). After 25 generations in the crowded cultures, the derived K-populations showed growth rate and productivity that at high densities were elevated relative to the controls, but at low density were depressed.

Animals↗

Ecological determinants of life-history evolution.

Density-dependent natural selection has been studied, empirically with laboratory populations of Drosophila melanogaster. Populations kept at very high and low population density have become differentiated with respect to important fitness-related traits. There is now some understanding of the behavioural and physiological basis of these differences. These studies have identified larval competitive ability and efficiency of food utilization as traits that are negatively correlated with respect to effects on fitness. Theory that illuminates and motivates additional research with this experimental system has been lacking. Current research has focused on models that incorporate many details of Drosophila ecology in laboratory environments.

Animals↗

Evolution of competitive ability in Drosophila by density-dependent natural selection.

The theory of density-dependent natural selection predicts that populations kept at extreme densities should evolve different competitive abilities for limited resources. These predictions have been tested with laboratory populations of Drosophila melanogaster. Six independent populations were maintained in two environments, called r and K, for 128 generations. In the r environment, population sizes were small and resources for larvae and adults were abundant. In contrast the populations in the K environment were large and crowded, and resources, such as food and space, were in short supply. The relative competitive ability for food has been estimated for each population. Populations from the K environment consume food at a rate that is 58% greater than the average rate for the r population. The differentiation of competitive abilities in these populations is due to natural selection and is consistent with predictions from the theory of evolutionary ecology.

Animals↗

Evolution of accelerated senescence in laboratory populations of Drosophila.

Ecological theories of life history evolution predict that natural selection should favor semelparous life histories in environments where juvenile survival is high relative to adult survival and rates of population growth are high. That is, organisms should complete their entire reproductive effort in a short period of time following maturation. Direct empirical verification of this idea has been lacking. Six independent populations of Drosophila melanogaster were maintained in two different environments, called r and K, for more than 120 generations. In the r environment population size was small, larval survival and rates of population growth were high, and reproduction was limited to a few days after eclosion. In the K environment population size was large and larval survival low, but adults were allowed to reproduce indefinitely. The fecundity of females of different sizes from each environment was measured daily for 4 weeks. No differences in fecundity were seen during the first week of adult life for females from the two environments. By the fourth week, however, the fecundity of large females from the r environment was 47-83% less than that of females from the K environment. The accelerated senescence exhibited by females from the r environment appears to be due to the accumulation of deleterious alleles whose effects are expressed late in life, which is consistent with the mutation accumulation hypothesis for the evolution of senescence.

Aging↗

A direct assessment of the role of genetic drift in determining allele frequency variation in populations of Euphydryas editha.

Estimates of allele frequencies at six polymorphic loci were collected over eight generations in two populations of Euphydryas editha. We have estimated, in addition, the effective population size for each generation for both populations with results from mark-recapture and other field data. The variation in allele frequencies generated by random genetic drift was then studied using computer simulations and our direct estimates of effective population size. Substantial differences between observed values and computer-generated expected values assuming drift alone were found for three loci (Got, Hk, Pgi) in one population. These observations are consistent with natural selection in a variable environment.

Alleles↗

Natural selection vs. random drift: evidence from temporal variation in allele frequencies in nature.

We have obtained monthly samples of two species, Drosophila pseudoobscura and Drosophila persimilis, in a natural population from Napa County, California. In each species, about 300 genes have been assayed by electrophoresis for each of seven enzyme loci in each monthly sample from March 1972 to June 1975. Using statistical methods developed for the purpose, we have examined whether the allele frequencies at different loci vary in a correlated fashion. The methods used do not detect natural selection when it is deterministic (e.g., overdominance or directional selection), but only when alleles at different loci vary simultaneously in response to the same environmental variations. Moreover, only relatively large fitness differences (of the order of 15%) are detectable. We have found strong evidence of correlated allele frequency variation in 13-20% of the cases examined. We interpret this as evidence that natural selection plays a major role in the evolution of protein polymorphisms in nature.

Alleles↗