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L Nunney

Publications and source records attributed to L Nunney.

12 recordsLinked to original sources
PubMed2007

Pupal period and adult size in Drosophila melanogaster: a cautionary tale of contrasting correlations between two sexually dimorphic traits.

Sexual dimorphism (SD) is widespread, reflecting a resolution of genetic conflicts arising from sex-specific differences in selection. However, genetic correlations among traits may constrain the evolution of SD. Drosophila melanogaster exhibits SD for pupal period (males longer) and adult weight (females heavier). This negative inter-sex covariance between the traits contrasts with a significant intra-sex positive genetic correlation (r(g) = 0.95) estimated using lines selected for fast larval development. Path analysis indicated that within sexes the selection regime indirectly reduced adult weight which in turn reduced pupal period. A hypothesis is proposed for the evolution of SD whereby the trait 'pupal period' is divided into 'intrinsic' (correlated with body size) and 'ecological' (uncorrelated with body size) components, and (the larger) females eclose earlier than males size via a shortening of the ecological component, thus achieving the advantage of provisioning eggs prior to sexual maturity. This hypothesis avoids invoking successful 'incompatible antagonistic selection'.

Analysis of Variance↗
PubMed2001

Increased sexual activity reduces male immune function in Drosophila melanogaster.

Despite the benefits of resistance, susceptibility to infectious disease is commonplace. Although specific susceptibility may be considered an inevitable consequence of the co-evolutionary arms race between parasite and host, a more general constraint may arise from the cost of an immune response. This "cost" hypothesis predicts a tradeoff between immune defense and other components of fitness. In particular, a tradeoff between immunity and sexually selected male behavior has been proposed. Here we provide experimental support for the direct phenotypic tradeoff between sexual activity and immunity by studying the antibacterial immune response in Drosophila melanogaster. Males exposed to more females showed a reduced ability to clear a bacterial infection, an effect that we experimentally link to changes in sexual activity. Our results suggest immunosuppression is an important cost of reproduction and that immune function and levels of disease susceptibility will be influenced by sexual selection.

Animals↗
PubMed2001

Selfish element maintains sex in natural populations of a parasitoid wasp.

Genomic conflicts between heritable elements with different modes of inheritance are important in the maintenance of sex and in the evolution of sex ratio. Generally, we expect sexual populations to exhibit a 1:1 sex ratio. However, because of their biology, parasitoid wasps often exhibit a female-biased sex ratio. Sex-ratio distorters can further alter this optimum, sometimes leading to the complete loss of sexual reproduction. In the parasitoid wasp Trichogramma kaykai ca. 4-26% of females in field populations are infected with a bacterial sex-ratio distorter, Wolbachia, allowing virgin mothers to produce daughters. In some micro-Hymenoptera these infections have led to the complete loss of sex, but in field populations of T. kaykai the proportion of individuals infected remains relatively stable. We tested several hypotheses to explain this low infection level, including inefficient and horizontal transmission of Wolbachia, suppressor genes negating the effect of Wolbachia and the presence of male-biasing sex-ratio distorters. Here, a male-biasing sex-ratio distorter, a parasitic B chromosome, causing females to produce only sons, keeps the frequency of Wolbachia low. The male-biasing factor of T. kaykai is the second known case of a B chromosome manipulating the reproduction of a parasitoid wasp.

Animals↗
PubMed2001

Geographic patterns of genetic differentiation within the restricted range of the endangered Stephens' kangaroo rat Dipodomys stephensi.

Using mtDNA variation in the kangaroo rat Dipodomys stephensi, we found no support for the hypothesis that a species with an historically restricted range will exhibit low levels of genetic polymorphism and little genetic structure. Dipodomys stephensi has long been restricted to a few interior coastal valleys in southern California encompassing an area of approximately 70 x 40 km; however, we found high levels of genetic variation over much of its range and significant genetic structure both within and between regions. We also found evidence for a recent range expansion. Dipodomys stephensi is a federally endangered species that is separated from D. panamintinus, its presumed sister taxon, by a mountain range to the north. We assessed genetic variation by sequencing 645 bases of the mitochondrial d-loop from 61 individuals sampled from 16 locations across the species range and rooted their relationship using two D. panamintinus individuals. Despite its limited geographic range, the level of mtDNA variation in D. stephensi is comparable to that of other rodents, including that of the more widely distributed D. panamintinus. This variation revealed significant regional differentiation. The northern, central, and southern regions of the range differ in both the level and the distribution of genetic variation. Phylogenetic analysis revealed that the center of the range contains the most diversity of lineages, including the most basal. In this region and in the north, most haplotypes were found at only a single location (25/29), or at a pair of nearby locations (3/29). In addition, related haplotypes clustered geographically. These results are consistent with long-term demographic stability characterized by limited dispersal and high local effective population size. Further support for this conclusion is the finding of unique diversity in two northern peripheral populations, Norco and Potrero Creek (PC). However, in sharp contrast, one haplotype (CC) was found at five of 11 central and northern locations and comprised 18% of individuals sampled. The atypical distribution of the CC haplotype reflected a pattern seen more strongly in the southern region. Here the CC haplotype comprised 69% of the sample and was found at all five sampling locations. Consequently, the southern region had very low genetic variability. We propose that this dominance of CC was probably due to a local population bottleneck that occurred during a recent range expansion into the southern region.

Animals↗
PubMed2000

Big houses, big cars, superfleas and the costs of reproduction.

The assumption of costs of reproduction were a logical necessity for much of the early development of life history theory. An unfortunate property of 'logical necessities' is that it is easy to also assume that they must be true. What if this does not turn out to be the case? The existence and universality of costs of reproduction were initially challenged with empirical data of questionable value, but later with increasingly strong theoretical and empirical results. Here, we discuss Ken Spitze's 'superfleas', which represent what we consider to be the strongest empirical challenge to the universality of costs, then offer a possible explanation for their existence.

Journal Article↗
PubMed1999

Lineage selection and the evolution of multistage carcinogenesis.

A wide array of proto-oncogenes and tumour suppressor genes are involved in the prevention of cancer. Each form of cancer requires mutations in a characteristic group of genes, but no single group controls all cancers. This lack of generality shows that the control of cancer is not an ancient, fixed property of cells. By contrast, it supports a dynamic evolutionary model, whereby genetic controls over unregulated cell growth are recruited independently through evolutionary time in different tissues within different taxa. The complexity of this genetic control can be predicted from a population genetic model of lineage selection driven by the detrimental fitness effects of cancer. Cancer occurs because the genetic control of cell growth is vulnerable to somatic mutations (or 'hits'), particularly in large, continuously dividing tissues. Thus, compared to small rodents, humans must have evolved more complex genetic controls over cell growth in at least some of their tissues because of their greater size and longevity; an expectation relevant to the application of mouse data to humans. Similarly, the 'two-hit' model so successfully applied to retinoblastoma, which originates in a small embryonic tissue, is unlikely to be generally applicable to other human cancers; instead, more complex scenarios are expected to dominate, with complexity depending upon a tissue's size and its pattern of proliferation.

Animals↗
PubMed1991

The influence of age structure and fecundity on effective population size.

Simple formulae are developed which define the effective size (Ne) of populations with overlapping generations, and their use is illustrated using data from a squirrel population. Two mating systems are considered, the random union of gametes and monogamy, in combination with age-independent fecundity. In the simplest case of age-independent (type 2) survivorship in a population of N adults, Ne = N/(2-T-1) where T is the generation time. As T increases, Ne declines asymptomatically to N/2. A generalization of this result (Ne = N/[1 + k-1-T-1], where k influences survivorship) shows that given type 1 survivorship (k greater than 1) this decline in Ne is less severe. A biased sex ratio results in Ne differing between the two mating systems; however, in both systems, a sex ratio bias resulting from survival differences has much less influence on Ne than a sex ratio bias resulting from recruitment differences. Low fecundity can increase Ne, but realistic levels of variation among breeding individuals (Poisson or greater) negate the effect. The effect on Ne of variation resulting from the presence of non-breeders is also considered.

Age Factors↗
PubMed1988

Factors influencing the optimum sex ratio in a structured population.

W. D. Hamilton (1967, Science 156, 477-488) calculated the optimum sex-ratio strategy for a population subdivided into local mating groups. He made three important assumptions: that the females founding each group responded precisely to the number of them initiating the group; that ail broods within a group matured synchronously; and that males were incapable of dispersing between groups. We have examined the effects of relaxing each of these assumptions and obtained the following results: (1) When broods mature asynchronously the optimum sex ratio is considerably more female biased than the Hamiltonian prediction. (2) Increasing male dispersal always decreases the optimum female bias to the sex ratio, but it is of particular interest that when moderate levels of dispersal are coupled with asynchrony of brood maturation then the optimum strategy is relatively insensitive to changes in foundress number. (3) When females cannot precisely determine the number of other foundresses initiating the group then the optimum strategy is almost exactly the strategy appropriate to a group of average size. These effects can be most easily understood in terms of local parental control (LPC) of the sex ratio. Through LPC a founding female can alter the mating success of her sons by altering the sex ratio of her brood. Asynchrony in the maturation of broods within a group increases the control that a founding female has over the mating success of her sons, whereas male dispersal reduces it. We have shown that the role of LPC and the role of inbreeding, which favors a female-biased sex ratio in haploidiploid species, are independent and that their effects can be combined into a single general formula r = (1-(r2/z2) E(alpha z/alpha r]/(1 + I). The concept of LPC can also be used to interpret two factors which have been proposed to select for the Hamiltonian sex ratios: local mate competition is LPC acting through sons; and sib mating is LPC acting through daughters.

Animals↗
PubMed1985

The effect of long time delays in predator-prey systems.

Past studies have indicated that a time delay longer than the natural period of a system will generally cause instability; however here it is shown that including long maturational time delays in a general predator-prey model need not have this effect. In each of the three cases studied (a predator delay, a prey delay, and both), local stability can persevere despite the presence of arbitrarily long time delays. This perseverence depends upon an interaction between delayed and undelayed features of the model. Delayed processes always act to destabilize the model. For example, prey self-regulation, usually a source of stability, becomes destabilizing if subject to a long delay. However, the effect of such a delay is offset by undelayed regulatory processes, such as a stabilizing functional response. In addition, the adverse effects of delayed predator recruitment can be reduced by the nonreproductive component of the numerical response, a feature not usually involved in determining stability. Finally, it is shown that long time delays are not necessarily more disruptive than short delays; it cannot be assumed that lengthening a time delay progressively reduces stability.

Aging↗