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International audience; At evolutionary equilibrium, ecological factors will determine the optimal combination of life-history trait values of an organism. This optimum can be assessed by assuming that the species maximizes some criterion of fitness such as the Malthusian coefficient or lifetime reproductive success depending on the degree of density-dependence. We investigated the impact of the amount of resources and habitat stability on a plant's age at maturity and life span by using an evolutionary optimization model in combination with empirical data. We conducted this study on sea beet, Beta vulgaris subsp. maritima, because of its large variation in life span and age at first reproduction along a latitudinal gradient including considerable ecological variation. We also compared the consequence in our evolutionary model of maximizing either the Malthusian coefficient or the lifetime reproductive success. Both the data analysis and the results of evolutionary modeling pointed to habitat disturbance and resources like length of the growing season as factors negatively related to life span and age at maturity in sea beet. Resource availability had a negative theoretical influence with the Malthusian coefficient as the chosen optimality criterion, while there was no influence in the case of lifetime reproductive success. As suggested by previous theoretical work the final conclusion on what criterion is more adequate depends on the assumptions of how in reality density-dependence restrains population growth. In our case of sea beet data R0 seems to be less appropriate than l.

Summary • Removal of developing fruits delays ageing in many annual plant species. This has long been seen as evidence that ageing is caused by resource depletion due to fruit development. Excision experiments can be interpreted from both evolutionary-ecology and resource-allocation viewpoints. Iteroparous (reproducing repeatedly) and annual plants may show different responses to excision. Furthermore, under the resource-depletion hypothesis, the more precocious the excision of reproductive organs, the greater the effect on allocation patterns. • A controlled-conditions experiment was set up involving six life cycles (from long-lived iteroparous to annual taxa of wild beets, Beta spp.) under three treatments of excision of reproductive-parts (buds, fruits and control). • Treatment effect was similar in semelparous and iteroparous beets, although effect on reproduction was more obvious in iteroparous ones. Flower-bud removal tended to induce resource allocation in new reproductive meristems, whatever the life cycle, without any effect on ageing in semelparous beets and probably none on survival in most iteroparous plants. Fruit removal had no effect. • These results and the occurrence of between-accessions variation are discussed in terms of the ecological significance of optimal allocation strategies.

Summary 1 Life span, an essential component of fitness, can be affected by traits such age at first reproduction, as well as by the mortality regime imposed by the environment. In a long-term experiment under controlled conditions, we studied life span in an iteroparous plant species, the sea beet Beta vulgaris ssp. maritima (L.), from 104 wild populations sampled in France, Belgium, Great Britain and the Netherlands. We estimated the intensity of selective pressures on life span and the specific effects of age at first reproduction (first or second year, depending on vernalization requirement) and of environmental disturbance. 2 Mean life span (measured in glasshouse conditions) increases with latitude from about 2 years in inland habitats of south-western France to at least 11 years in north Brittany, before decreasing to about 5 years in the northernmost populations. 3 Comparison of spatial autocorrelograms for life span and cytoplasmic neutral markers showed there is strong selection for life span. 4 Within populations the effect of age at first reproduction on life span proved to be marginal. No causal relationship was detected among populations, although, in the southern part of the study area, a strong association between reproduction in the first year and short life span suggests common selective pressures. 5 Life span appeared to be highly associated with habitat type, as defined by mortality regimes. Populations with the longest-lived individuals occurred in the most stable habitats and populations with the shortest-lived individuals in the most disturbed locations.

Summary 1 Long-distance dispersal events are biologically very important for plants because they affect colonization probabilities, the probabilities of population persistence in a fragmented habitat, and metapopulation structure. They are, however, very difficult to investigate because of their low frequency. We reviewed the use of molecular markers in the population genetics approach to studying dispersal. With these methods the consequences of long-distance dispersal are studied, rather than the frequency of the dispersal events themselves. 2 Molecular markers vary, displaying different amounts of variation and different modes of inheritance: they may be either dominant or codominant, and may or may not be subjected to genetic recombination. Use of markers has inspired the development of maximum likelihood techniques that take the evolutionary history of alleles into account while estimating gene flow. 3 Inferring seed dispersal rates from indirect measurements of gene flow involves three steps: (i) quantifying genetic differentiation among populations and using this to estimate the rate of gene flow; (ii) producing a genetic dispersal curve by regressing geographical distance among populations against the amount of gene flow; and (iii) separating seed-mediated from pollen-mediated gene flow, by comparing differentiation in nuclear vs. cytoplasmic molecular markers. In this way, potentially very low levels of gene flow can be detected. 4 The indirect approach is based on a number of assumptions. The validity of each assumption should be assessed by independent methods or the estimates of gene flow and dispersal should be mainly used in a comparative context. In metapopulations, with frequent extinction and colonization, the relationship between genetic differentiation and gene flow is not straightforward, and other methods should be used. 5 Highly variable molecular markers, especially microsatellites, have facilitated a direct genetic approach to measuring gene flow, based on parental analyses. 6 The population genetic approach provides different information about dispersal than ecological methods. Thus population genetic and ecological methods may supplement each other, and together lead to a better insight into the dispersal process than either of the methods on its own.