Are adaptation costs necessary to build up a local adaptation pattern?

<p>Abstract</p> <p>Background</p> <p>Ecological specialization is pervasive in phytophagous arthropods. In such specialization mode, limits to host range are imposed by trade-offs preventing adaptation to several hosts. The occurrence of such trade-offs is inferred by a pattern of local adaptation, i.e., a negative correlation between relative performance on different hosts.</p> <p>Results</p> <p>To establish a causal link between local adaptation and trade-offs, we performed experimental evolution of spider mites on cucumber, tomato and pepper, starting from a population adapted to cucumber. Spider mites adapted to each novel host within 15 generations and no further evolution was observed at generation 25. A pattern of local adaptation was found, as lines evolving on a novel host performed better on that host than lines evolving on other hosts. However, costs of adaptation were absent. Indeed, lines adapted to tomato had similar or higher performance on pepper than lines evolving on the ancestral host (which represent the initial performance of all lines) and the converse was also true, e.g. negatively correlated responses were not observed on the alternative novel host. Moreover, adapting to novel hosts did not result in decreased performance on the ancestral host. Adaptation did not modify host ranking, as all lines performed best on the ancestral host. Furthermore, mites from all lines preferred the ancestral to novel hosts. Mate choice experiments indicated that crosses between individuals from the same or from a different selection regime were equally likely, hence development of reproductive isolation among lines adapted to different hosts is unlikely.</p> <p>Conclusion</p> <p>Therefore, performance and preference are not expected to impose limits to host range in our study species. Our results show that the evolution of a local adaptation pattern is not necessarily associated with the evolution of an adaptation cost.</p

Darwin’s wind hypothesis: does it work for plant dispersal in fragmented habitats?

Using the wind-dispersed plant Mycelis muralis, we examined how landscape fragmentation affects variation in seed traits contributing to dispersal. Inverse terminal velocity (Vt−1) of field-collected achenes was used as a proxy for individual seed dispersal ability. We related this measure to different metrics of landscape connectivity, at two spatial scales: in a detailed analysis of eight landscapes in Spain and along a latitudinal gradient using 29 landscapes across three European regions. In the highly patchy Spanish landscapes, seed Vt−1 increased significantly with increasing connectivity. A common garden experiment suggested that differences in Vt−1 may be in part genetically based. The Vt−1 was also found to increase with landscape occupancy, a coarser measure of connectivity, on a much broader (European) scale. Finally, Vt−1 was found to increase along a south–north latitudinal gradient. Our results for M. muralis are consistent with ‘Darwin’s wind dispersal hypothesis’ that high cost of dispersal may select for lower dispersal ability in fragmented landscapes, as well as with the ‘leading edge hypothesis’ that most recently colonized populations harbour more dispersive phenotypes.

Genetic, ecological, behavioral and geographic differentiation of populations in a thistle weevil: implications for speciation and biocontrol

Because weevils are used as biocontrol agents against thistles, it is important to document and understand host shifts and the evolution of host-specificity in these insects. Furthermore, such host shifts are of fundamental interest to mechanisms of speciation. The mediterranean weevil Larinus cynarae normally parasitizes either one of two thistle genera, Onopordum and Cynara, being locally monophagous. In Sardinia, however, both host genera are used. We used three types of data to help understand this complex host use: (i) weevil attack rates on the two host genera among 53 different populations in Sardinia and nearby Corsica, (ii) host preference in a lab setting, and (iii) genetic (allozyme) differentiation among weevil populations exploiting the same or different hosts. Using a subset of populations from northern Sardinia, we attempted to relate interpopulation differences in host preference to gene flow among populations by comparing pairwise differences in oviposition preference (Qst) and in allozyme frequencies (Fst). Overall, Qst and Fst were positively correlated. Fst was positively correlated with geographic distance among pairs of populations using the same host, but not among different-host population pairs. As mating occurs on the hosts, this result suggests reinforcement. Genetic evidence indicates Cynara as the ancestral host of the weevils from both islands and our current studies suggest repeated attempts to colonize Onopordum, with a successful shift in Corsica and a partial shift in Sardinia. This scenario would explain why in Sardinia the level of attack was higher on Cynara than on Onopordum and why, when given a choice in the laboratory, Sardinian weevils preferred Cynara even when sampled from Onopordum. The lability of host shifts in L. cynarae supports caution in using these or related weevils as biocontrol agents of exotic thistles

De la métapopulation au voisinage: la génétique des populations en déséquilibre

Tribune LibreInternational audienceThe concept of population is very useful but can sometimes lead to dead ends. Indeed, various questions in population genetics cannot be solved if studied at this level. It is shown that the intensity of dispersion, as far as it is genetically determined, does not respond to selection at the level of the population in its usual sens. A simple theorical model in relation with in-situ observations (on carduus), seems to show that a wider set, the matapopulation (Gill), is necessary to account for the processes concerned. From this viewpoint, instead of considering species as sets of independent populations, it is proposed to consider them as sets of metapopulations where individual populations are regulary founded by the others and then evolve under internal pressures. Are these internal pressures acting at the very population level ? It does not seem so, at least for some, and perhaps for most species, since each individual is likely to mate with a subset which is not representative of the whole. This question has led Wright to formulate the neighbourhood concept. In Thyme, the simultaneous integration of the emerging properties of the 3 levels (Metapopulation, Population and Neighbourhood) allows one to explain a phenomenon (very high proportions of females) which remained incomprehensible as long as one tried to describe it using only the population level