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Genetic Cost (genetic + cost)
Selected AbstractsSix costs of immunity to gastrointestinal nematode infectionsPARASITE IMMUNOLOGY, Issue 2 2008I. G COLDITZ SUMMARY The strength of the immune response and the outcome of the interaction of a host with a parasite are influenced by genetic and phenotypic characteristics of both parties, and by environmental variables. Allocation of host resources to immune defence reduces resources available for other life-history traits. This review identifies six potential costs to the host from immune activation. The costs are likely to be broadly applicable to other immune responses in vertebrate species. Five phenotypic costs arise from: (i) increased metabolic activity; (ii) reduced nutrient availability due to anorexia; (iii) altered priorities for nutrient utilization; (iv) change in size and turnover of pools of immune cells and proteins; and (v) immunopathology from inappropriate or excessive immune activation. Subsumed by these costs is the cost of altered efficiency of nutrient use. A sixth cost is the genetic cost which arises from a change in the capacity of offspring to express production and life-history traits following selection for parasite resistance. The sensitivity of immune responses to the phenotypic status of the host, and the role the immune system shares with the neuroendocrine system in controlling use of resources underpin the importance of immunocompetence to the life-history of the host. [source] Modelling binary mixtures of herbicides in populations resistant to one of the components: evaluation for resistance managementPEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 2 2009Bertrand Jacquemin Abstract BACKGROUND: Herbicide mixtures are commonly proposed to delay the selection of herbicide resistance in susceptible populations (called the SM strategy). However, in practice, herbicide mixtures are often used when resistance to one of the two active ingredients has already been detected in the targeted population (called the RM strategy). It is doubtful whether such a practice can select against resistance, as the corresponding selection pressure is still exerted. As a consequence, the effect of mixtures on the evolution of an already detected resistance to one of the herbicides in the combination remains largely unexplored. In the present work, a simple model was developed to explore further the necessary and sufficient conditions under which a binary RM strategy might stabilise or even reduce resistance frequency. RESULTS: Covering the hypothetical largest range of parameters, 39% of 9000 random simulations attest that the RM strategy might theoretically reduce resistance frequency. When strong enough, high genetic cost of resistance, negative cross-resistance between the herbicides associated in the mixture and reduced selection differential between resistant and susceptible plants can counterbalance the resistance advantage to one of the two applied herbicides. However, the required conditions for an RM strategy to ensure resistance containment in natural conditions seldom overlap with experimental parameter estimates given in the literature. CONCLUSION: It is concluded that the sufficient conditions for an RM strategy to be effective would rarely be encountered. As a consequence, the strategy of formulating mixtures with herbicides for which resistance has already been detected should be avoided. Copyright © 2008 Society of Chemical Industry [source] THE ADAPTIVE DYNAMICS OF ALTRUISM IN SPATIALLY HETEROGENEOUS POPULATIONSEVOLUTION, Issue 1 2003JEAN-FRANÇOIS LE GALLIARD Abstract., We study the spatial adaptive dynamics of a continuous trait that measures individual investment in altruism. Our study is based on an ecological model of a spatially heterogeneous population from which we derive an appropriate measure of fitness. The analysis of this fitness measure uncovers three different selective processes controlling the evolution of altruism: the direct physiological cost, the indirect genetic benefits of cooperative interactions, and the indirect genetic costs of competition for space. In our model, habitat structure and a continuous life cycle makes the cost of competing for space with relatives negligible. Our study yields a classification of adaptive patterns of altruism according to the shape of the costs of altruism (with decelerating, linear, or accelerating dependence on the investment in altruism). The invasion of altruism occurs readily in species with accelerating costs, but large mutations are critical for altruism to evolve in selfish species with decelerating costs. Strict selfishness is maintained by natural selection only under very restricted conditions. In species with rapidly accelerating costs, adaptation leads to an evolutionarily stable rate of investment in altruism that decreases smoothly with the level of mobility. A rather different adaptive pattern emerges in species with slowly accelerating costs: high altruism evolves at low mobility, whereas a quasi-selfish state is promoted in more mobile species. The high adaptive level of altruism can be predicted solely from habitat connectedness and physiological parameters that characterize the pattern of cost. We also show that environmental changes that cause increased mobility in those highly altruistic species can beget selection-driven self-extinction, which may contribute to the rarity of social species. [source] A phallus for free?JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 1 2003Quantitative genetics of sexual trade-offs in the snail Bulinus truncatus Abstract Resource allocation is thought to play a key role in the coexistence of different sexual morphs within hermaphroditic species. Indeed, most models assume that sexual functions are subject to a balance between reproductive advantage and energetic cost. Various types of cost (e.g. organ construction, maintenance and utilization) and levels of trade-off (physiological and genetic) may be considered. We here examine physiological and genetic costs of phallus construction and maintenance in Bulinus truncatus, a snail species in which aphallic individuals (without phallus) coexist with regular hermaphrodites. We use a quantitative genetic design involving 37 inbred lines (four populations) known to produce different proportions of aphallics, to test for the existence of genetic and nongenetic correlations between aphally and a range of life-history traits over the totality of the life cycle. Our results show that aphallic and euphallic individuals of the same line do not show consistent differences in either growth, fecundity (including offspring survival), or longevity. Furthermore, none of these traits is genetically correlated across lines with the frequency of the aphallic morph. We conclude that the cost of the construction and maintenance of the phallus must be very low in this species. Future studies should investigate the cost associated with using the phallus (i.e. male outcrossing behaviour) to explain the maintenance of high frequencies of aphallic individuals in natural populations. [source] | ||||||||||