Plant traits have been widely used to characterize different aspects of the ecology of plant species. Despite its wide distribution and its proven significance at the level of individuals, communities, and populations, the ability to form mycorrhizal associations has been largely neglected in these studies so far. Analyzing plant traits associated with the occurrence of mycorrhizas in plants can therefore enhance our understanding of plant strategies and distributions. Using a comparative approach, we tested for associations between mycorrhizal status and habitat characteristics, life history traits, and plant distribution patterns in 1752 species of the German flora (a major part of the Central European flora). Data were analyzed using log-linear models or generalized linear models, both accounting for phylogenetic relationships. Obligatorily mycorrhizal (OM) species tended to be positively associated with higher temperature, drier habitats, and higher pH; and negatively associated with moist, acidic, and fertile soils. Competitive species were more frequently OM, and stress tolerators were non-mycorrhizal (NM), while ruderal species did not show any preference. Facultatively mycorrhizal (FM) species showed the widest geographic and ecological amplitude. Indigenous species were more frequently FM and neophytes (recent aliens) more frequently OM than expected. FM species differed markedly from OM and NM species in almost all analyzed traits. Specifically, they showed a wider geographic distribution and ecological niche. Our study of the relationships between mycorrhizal status and other plant traits provides a comprehensive test of existing hypotheses and reveals novel patterns. The clear distinction between FM and OM + NM species in terms of their ecology opens up a new field of research in plant-mycorrhizal ecology.

Summary• Communities of arbuscular mycorrhizal (AM) fungi were characterized in roots of rare Pulsatilla patens and common P. pratensis native adults and seedlings grown in soils from Estonian boreal forest and grassland habitats. Since establishment of Pulsatilla species predominantly occurs in vegetation-free gaps, seedling baiting experiments were aimed at gap simulation.• The AM fungal small subunit ribosomal RNA gene (SSU rDNA) sequences amplified from roots were subjected to denaturing gradient gel electrophoresis (DGGE), cloning, restriction fragment length polymorphism (RFLP) grouping, sequence phylogenetic and multivariate analyses.• Nineteen identified sequence groups comprised 14 putative Glomus , two Acaulospora , two Scutellospora and one Gigaspora groupings. Four and six groupings, respectively, contained previously described species and root-derived AM fungal sequences. Sequence groups were identified in seedling roots that were more abundant in a grassland ( Glomus sp. MO-G3) or a forest soil ( Glomus spp. MO-G2 and MO-G5).• Our data showed site-dependent differences in AM fungal community composition, but we failed to identify AM fungi specifically or preferentially colonizing the rare plant species.

* Here, the diversity of arbuscular mycorrhizal (AM) fungi was determined in a boreal herb-rich coniferous forest in relation to environmental variables. * Root samples of five plant species (Fragaria vesca, Galeobdolon luteum, Hepatica nobilis, Oxalis acetosella and Trifolium pratense) were analysed from stands differing in age and forest management intensity. * Thirty-four Glomeromycota taxa (small-subunit ribosomal RNA gene (SSU rDNA) sequence groups) were detected from 90 root samples (911 clones), including eight new taxa. Sequence groups related to Glomus intraradices were most common (MO-G3 and MO-G13). Samples of H. nobilis were colonized by more AM fungal taxa (3.68 +/- 0.31) than those of O. acetosella (2.69 +/- 0.34), but did not differ significantly in this respect from those of F. vesca (3.15 +/- 0.38). Effects of forest management, host plant species (except above) or season on the number or composition of fungal taxa in root samples were not detected, and neither were they explained by environmental variables (vegetation, soil and light conditions). * This is the most taxon-rich habitat described to date in terms of root-colonizing Glomeromycota. The data demonstrate the importance of temperate coniferous forests as habitats for AM fungi and plants. Lack of obvious fungal community patterns suggests more complex effects of biotic and abiotic factors, and possibly no adverse effect of common forest management practices on AM fungal diversity.

To evaluate the relative roles of seed availability and competitive interactions in creating within-community patterns of species richness in unproductive grassland, we conducted a sowing experiment in a dry calcareous (alvar) grassland, where both the number of arriving seeds and the number of arriving species were approximately doubled compared to the natural seed rain. Also, in half of the plots, 36% of the vegetation and bryophyte cover was removed to simulate disturbance. Sowing significantly increased species richness and the number of seedlings in plots. Disturbance increased the number of seedlings but had no significant effect on species richness. In the first year, the highest number of seedlings was found in disturbed and sown plots. The dynamics of seedling numbers differed among species. Of the 15 sown species, seedlings of nine species were found in some plots. The number of seedlings of two species were not dependent on treatments, those of three species depended only on sowing, and for four species there was a significant positive interaction between sowing and disturbance. The establishment of sown species was not dependent on initial species richness or number of adult ramets in experimental plots. It was concluded that, though the behavior of individual species may differ, the local deficiency of seeds may be an important force generating small-scale community patterns of calcareous grasslands.

We were interested in the role of arbuscular mycorrhiza (AM) in the competition between plants of different sizes. A pot experiment of factorial design was established, in which AM root colonization and competition were used as treatments. Five-week-old Prunella vulgaris seedlings were chosen as target plants (i.e. plants whose response to competition was studied) and the following (13 replicates of each) were used as neighbours: (1) a large, 10-week-old P. vulgaris, (2) two P. vulgaris seedlings, and (3) a large, 10-week-old Fragaria vesca. In the experiment where small neighbours were grown together with small target plants, competition did not reduce target plant weight significantly, compared to the other two treatments. The competitive effects of large neighbours were significant, regardless of species (both older neighbours reduced the weights of target plants similarly), but there was a clear difference between intra- and interspecific competition when plants were mycorrhizal. In intraspecific competition with a large neighbour, the target plant shoot weight was reduced 24% when inoculated with AM. Thus, AM amplified rather than balanced intraspecific competition. In interspecific competition with old F. vesca, the shoot weights of target plants were 22% greater when inoculated with AM than when non-mycorrhizal. The results showed that, for given soil condition, AM might increase species diversity by increasing competitive intraspecific suppression and decreasing the interspecific suppression of small plants by larger neighbours.