No abstract

Stoloniferous rosette plants may show horizontal and vertical foraging responses, such as changes in branching frequency, stolon internode length, leaf length, and height growth of stolons. To study whether such plastic foraging responses constitute an adaptation to heterogeneity in competition, we studied genetic variation in and fitness consequences of plastic foraging responses in the stoloniferous lake-shore plant Ranunculus reptans. Because plastic foraging responses are likely to have been more strongly selected for in heterogeneous environments, we used 15 genotypes from competitive, heterogeneous microhabitats and 15 from competition-free, homogeneous microhabitats from Lake Constance (central Europe).We planted vegetatively propagated rosettes of the 30 genotypes (totaling 236 rosettes) into a greenhouse environment with spatially heterogeneous competition. Four replicates of each genotype were planted into the competition-free halves of experimental trays, and four other replicates into the halves with the naturally co-occurring grass Agrostis stolonifera.We found significant variation among genotypes in vertical and horizontal foraging responses. In line with the hypothesis of adaptive plasticity, genotypes from the competitive heterogeneous microhabitats more strongly increased the vertical angle of the first stolon internode (126%) and the specific stolon length (166%) in response to competition than genotypes from the competition-free homogeneous microhabitats. Moreover, we found that genotypes that were more plastic in the vertical angle of the first stolon internode, stolon height, and specific internode length produced more rosettes and flowers than less plastic genotypes (all selection gradients for plasticity Ͼ 0.316).Our findings strongly suggest that plastic foraging responses constitute an adaptation to environmental heterogeneity, at least in the stoloniferous R. reptans.

In clonal plants, evolution of plastic foraging by increased lengths of leaves and internodes under unfavourable conditions may be constrained by costs and limits of plasticity. We studied costs and limits of plasticity in foraging characteristics in 102 genotypes of the stoloniferous herb Ranunculus reptans. We grew three replicates of each genotype with and three without competition by the naturally co-occuring grass Agrostis stolonifera. We used regression and correlation analyses to investigate potential costs of plasticity in lengths of leaves and stolon internodes, developmental instability costs of these traits, and a developmental range limit of these traits. We used randomization procedures to control for spurious correlations between parameters calculated from the same data. Under competition the number of rosettes, rooted rosettes, and flowers was 58%, 40%, and 61% lower, respectively, than in the absence of competition. Under competition lengths of leaves and stolon internodes were 14% and 6% smaller, respectively, than in the absence of competition. We detected significant costs of plasticity in stolon internode length in the presence of competition when fitness was measured in terms of the number of rosettes and the number of flowers (selection gradients against plasticity were 0.250 and 0.214, respectively). Within-environment variation (SD) in both foraging traits was not positively correlated with the corresponding plasticity, which indicates that there were no developmental instability costs. More plastic genotypes did not have less extreme trait values than less plastic genotypes for both foraging traits, which indicates that there was no developmental range limit. We conclude that in R. reptans costs of plasticity more strongly constrain evolution of foraging in the horizontal plane (i.e., stolon internode length) than in the vertical plane (i.e., leaf length).

Abstract. Allocation to sexual reproduction is an important life-history trait in clonal plants. Different selection pressures between competitive and competition-free environments are likely to result in the evolution of specialized genotypes and to maintain genetic variation in reproductive allocation. Moreover, selection may also result in the evolution of plastic allocation strategies. The necessary prerequisite for evolution, heritable genetic variation, can best be studied with selection experiments. Starting from a base population of 102 replicated genotypes of the clonal herb Ranunculus reptans, we imposed selection on the proportion of flowering rosettes in the absence of competition (base population: mean ϭ 0.391, broad-sense heritability ϭ 0.307). We also selected on the plasticity in this trait in response to competition with a naturally coexisting grass in a parallel experiment (base population: 14% lower mean in the presence of competition, broad-sense heritability ϭ 0.072). After two generations of bidirectional selection, the proportion of flowering rosettes was 26% higher in the high line than in the low line (realized heritability Ϯ SE ϭ 0.205 Ϯ 0.017). Moreover, genotypes of the high line had 11% fewer carpels per flower, a 22% lower proportion of rooted rosettes, and a 39% smaller average distance between rosettes within a clone. In the second experiment, we found no significant responses to selection for high and low plasticity in the proportion of flowering rosettes (realized heritability Ϯ SE ϭ Ϫ0.002 Ϯ 0.013). Our study indicates a high heritability and potential for further evolution of the proportion of flowering rosettes in R. reptans, but not for its plasticity, which may have been fixed by past evolution at its current level. Moreover, our results demonstrate strong genetic correlations between allocation to sexual reproduction and other clonal life-history characteristics.

Regional species assemblages have been shaped by colonization, speciation and extinction over millions of years. Humans have altered biogeography by introducing species to new ranges. However, an analysis of how strongly naturalized plant species (i.e. alien plants that have established self-sustaining populations) affect the taxonomic and phylogenetic uniqueness of regional floras globally is still missing. Here, we present such an analysis with data from native and naturalized alien floras in 658 regions around the world. We find strong taxonomic and phylogenetic floristic homogenization overall, and that the natural decline in floristic similarity with increasing geographic distance is weakened by naturalized species. Floristic homogenization increases with climatic similarity, which emphasizes the importance of climate matching in plant naturalization. Moreover, floristic homogenization is greater between regions with current or past administrative relationships, indicating that being part of the same country as well as historical colonial ties facilitate floristic exchange, most likely due to more intensive trade and transport between such regions. Our findings show that naturalization of alien plants threatens taxonomic and phylogenetic uniqueness of regional floras globally. Unless more effective biosecurity measures are implemented, it is likely that with ongoing globalization, even the most distant regions will lose their floristic uniqueness.

Abstract. Clonal plant life histories are special in at least four respects: (I) Clonal plants can also reproduce vegetatively, (2) vegetative reproduction can be realised with short or long spacers, (3) a nd it may allow to plastically place vegetative offspring in benign patches. (4) Moreover, ramets of clonal plants may remain physically and physiologically integrated. Because of the apparent utility of such traits and because ecological patterns of distribution of clonal and non clonal plants differ, adaptation is a tempting explanation of observed clonal life history variation. However, adaptivc evolution requires (I) heri table genetic variation and (2) a trait effect on fitness, a nd (3) it may be cons trained if other evolutionary forces are overriding selection or hy constraints, costs and trade offs. (I) The few studies undertaken so far reported broad sense heritability for clonal traits. Variation in selectively neutral genetic markers appears as pronounced in popu lations of clonal as non clonal plants. However, neutral markers may not reflect heritable variation of life history traits . Moreover, clonal plants may have been samp led at larger spatia l scales. Empirical information on the contribution of somatic mutations to heritable variation is lacking.(2) C lonal life hi sto ry traits were found to affect fitness. However, much of this evidence stems from artificial rather than natura l environments. (3) The relative importance of gene flow, inbreeding, and genetic drift, compared with selection, in the evo lution of clonal life histories is hardly explored. Benefits of clonal life history traits were frequently studied a nd found. How ever, there is a lso evidence for constraints, trade offs, and costs. In conclusion, though it is very likely, that clonal life history traits are adaptive, it is neither clear to which degree this is the case, nor which clonal life history traits constitute adaptat io ns to which environmenta l fac tors. Moreover, evo lutionary interactions among clonal life history traits and between clonal and non clonal ones, such as the mating sys tem, are not well explored. There remains much interesting work to be done in this field which will be particularly interesting if it is done in the field.

In clonal plants, evolution of plastic foraging by increased lengths of leaves and internodes under unfavourable conditions may be constrained by costs and limits of plasticity. We studied costs and limits of plasticity in foraging characteristics in 102 genotypes of the stoloniferous herb Ranunculus reptans. We grew three replicates of each genotype with and three without competition by the naturally co-occuring grass Agrostis stolonifera. We used regression and correlation analyses to investigate potential costs of plasticity in lengths of leaves and stolon internodes, developmental instability costs of these traits, and a developmental range limit of these traits. We used randomization procedures to control for spurious correlations between parameters calculated from the same data. Under competition the number of rosettes, rooted rosettes, and flowers was 58%, 40%, and 61% lower, respectively, than in the absence of competition. Under competition lengths of leaves and stolon internodes were 14% and 6% smaller, respectively, than in the absence of competition. We detected significant costs of plasticity in stolon internode length in the presence of competition when fitness was measured in terms of the number of rosettes and the number of flowers (selection gradients against plasticity were 0.250 and 0.214, respectively). Within-environment variation (SD) in both foraging traits was not positively correlated with the corresponding plasticity, which indicates that there were no developmental instability costs. More plastic genotypes did not have less extreme trait values than less plastic genotypes for both foraging traits, which indicates that there was no developmental range limit. We conclude that in R. reptans costs of plasticity more strongly constrain evolution of foraging in the horizontal plane (i.e., stolon internode length) than in the vertical plane (i.e., leaf length).

Allocation to sexual reproduction is an important life-history trait in clonal plants. Different selection pressures between competitive and competition-free environments are likely to result in the evolution of specialized genotypes and to maintain genetic variation in reproductive allocation. Moreover, selection may also result in the evolution of plastic allocation strategies. The necessary prerequisite for evolution, heritable genetic variation, can best be studied with selection experiments. Starting from a base population of 102 replicated genotypes of the clonal herb Ranunculus reptans, we imposed selection on the proportion of flowering rosettes in the absence of competition (base population: mean = 0.391, broad-sense heritability = 0.307). We also selected on the plasticity in this trait in response to competition with a naturally coexisting grass in a parallel experiment (base population: 14% lower mean in the presence of competition, broad-sense heritability = 0.072). After two generations of bidirectional selection, the proportion of flowering rosettes was 26% higher in the high line than in the low line (realized heritability +/- SE = 0.205 +/- 0.017). Moreover, genotypes of the high line had 11% fewer carpels per flower, a 22% lower proportion of rooted rosettes, and a 39% smaller average distance between rosettes within a clone. In the second experiment, we found no significant responses to selection for high and low plasticity in the proportion of flowering rosettes (realized heritability +/- SE = -0.002 +/- 0.013). Our study indicates a high heritability and potential for further evolution of the proportion of flowering rosettes in R. reptans, but not for its plasticity, which may have been fixed by past evolution at its current level. Moreover, our results demonstrate strong genetic correlations between allocation to sexual reproduction and other clonal life-history characteristics.