Similarity of introduced plant species to native ones facilitates naturalization, but differences enhance invasion success

The search for traits associated with plant invasiveness has yielded contradictory results, in part because most previous studies have failed to recognize that different traits are important at different stages along the introduction–naturalization–invasion continuum. Here we show that across six different habitat types in temperate Central Europe, naturalized non-invasive species are functionally similar to native species occurring in the same habitat type, but invasive species are different as they occupy the edge of the plant functional trait space represented in each habitat. This pattern was driven mainly by the greater average height of invasive species. These results suggest that the primary determinant of successful establishment of alien species in resident plant communities is environmental filtering, which is expressed in similar trait distributions. However, to become invasive, established alien species need to be different enough to occupy novel niche space, i.e. the edge of trait space

Refugial occurrence and ecology of the land snail Vertigo lilljeborgi in fen habitats in temperate mainland Europe

Vertigo lilljeborgi (Westerlund, 1871) is one of the rarest terrestrial snail species in temperate mainland Europe, traditionally considered a glacial relict there. This contrasts with its occurrence in northern Europe where it is a widespread species. This species prefers constantly wet habitats that are neutral to slightly acidic, and avoids highly alkaline conditions, which is an extremely rare ecology for a Eurasian mollusc. Until 2012, only five historical records of this species were known in mainland Europe to the south of its main distribution in northern Europe. Since then, 20 new sites have been discovered, mostly located in the Hercynian Mountains (Bohemian Massif in the Czech Republic and Massif Central in France). In comparison with the boreal European and Alpine populations, those from the Hercynian Mountains inhabit acidic, rather soligenous and productive fens, strongly dominated by Sphagnum. Vertigo lilljeborgi does not occur in some sites with apparently suitable habitats as indicated by species composition of the vegetation. We observed a surprising correspondence between the occurrence of V. lilljeborgi and mean July air temperature and we report its first fossil record from the last glacial period from Central Europe. Although the number of its sites has increased recently, these sites represent unusual and highly unique habitats, vulnerable to drainage and destruction from human activities. This calls for a need of conservation efforts in most of the newly discovered isolated sites

Macroevolutionary patterns in European vegetation

Question Habitat‐specific species pools are shaped by ecological and evolutionary processes such as speciation, extinction, and migration. However, their role is poorly known because of the lack of robust data on species pools across a large number of plant community types and large areas. Here, we analyse a unique dataset of species pools of diagnostic species for all European vegetation types, asking: (a) what are the patterns of phylogenetic structure and phylogenetic beta‐diversity across European vegetation types and biomes; (b) what are the drivers of these patterns; and (c) is there a signal of niche conservatism at the level of biomes and broad categories of vegetation types? Location Europe, Canary Islands, Madeira, Azores, Cyprus, Caucasus, Iceland and Greenland. Methods We built a dataset comprising 10,804 vascular plant species (almost 85% of the European flora) assigned to 106 vegetation types representing all European vegetated habitats, grouped into 11 biomes. This dataset represented habitat‐specific species pools. We analysed the phylogenetic structure of the species pools and related it to distribution range sizes of individual vegetation types, their successional status, levels of disturbance and environmental stress. Results In European vegetation, phylogenetic overdispersion is associated with late‐successional habitats: several forest types, aquatic vegetation, and rock‐cliff vegetation serve as depositories of relict lineages. In contrast, phylogenetic clustering is typical of early successional and disturbed vegetation in anthropogenic, coastal and saline habitats, and in open‐canopy Mediterranean vegetation. The phylogenetic similarity of vegetation types is higher within than between broad categories of vegetation types and biomes. Conclusions The variable phylogenetic structure of European vegetation types is a heritage of evolutionary processes in the Tertiary and Quaternary. Habitat‐specific species pools of different vegetation types and biomes have been formed by different evolutionary processes as indicated by the observation that certain clades are significantly associated with certain vegetation types or biomes, hence indicating the phylogenetic niche conservatism

Alpha diversity of vascular plants in European forests

Aim The former continental‐scale studies modelled coarse‐grained plant species‐richness patterns (gamma diversity). Here we aim to refine this information for European forests by (a) modelling the number of vascular plant species that co‐occur in local communities (alpha diversity) within spatial units of 400 m2; and (b) assessing the factors likely determining the observed spatial patterns in alpha diversity. Location Europe roughly within 12°W–30°E and 35–60°N. Taxon Vascular plants. Methods The numbers of co‐occurring vascular plant species were counted in 73,134 georeferenced vegetation plots. Each plot was classified by an expert system into deciduous broadleaf, coniferous or sclerophyllous forest. Random Forest models were used to map and explain spatial patterns in alpha diversity for each forest type separately using 19 environmental, land‐use and historical variables. Results Our models explained from 51.0% to 70.9% of the variation in forest alpha diversity. The modelled alpha‐diversity pattern was dominated by a marked gradient from species‐poor north‐western to species‐rich south‐eastern Europe. The most prominent richness hotspots were identified in the Calcareous Alps and adjacent north‐western Dinarides, the Carpathian foothills in Romania and the Western Carpathians in Slovakia. Energy‐related factors, bedrock types and terrain ruggedness were identified as the main variables underlying the observed richness patterns. Alpha diversity increases especially with temperature seasonality in deciduous broadleaf forests, on limestone bedrock in coniferous forests and in areas with low annual actual evapotranspiration in sclerophyllous forests. Main conclusions We provide the first predictive maps and analyses of environmental factors driving the alpha diversity of vascular plants across European forests. Such information is important for the general understanding of European biodiversity. This study also demonstrates a high potential of vegetation‐plot databases as sources for robust estimation of the number of vascular plant species that co‐occur at fine spatial grains across large areas.M.V., J.D., I.K., M.Ř. and M.C. were supported by the Czech Science Foundation (Centre of Excellence Pladias; project no. 14–36079G). I.B. and J.A.C. were supported by the Basque Government (IT936‐16). B.J.‐A. was supported by the Marie Curie Clarín‐COFUND program of the Principate of Asturias and the European Union (ACB17‐26). J.‐C.S. considers this work a contribution to his VILLUM Investigator project “Biodiversity Dynamics in a Changing World” funded by VILLUM FONDEN (grant 16549) and his Danish Council for Independent Research | Natural Sciences TREECHANGE project (grant 6108‐00078B)

Mapping species richness of plant families in European vegetation

Aims Biodiversity is traditionally studied mostly at the species level, but biogeographical and macroecological studies at higher taxonomic levels can provide valuable insights into the evolutionary processes at large spatial scales. Our aim was to assess the representation of vascular plant families within different vegetation formations across Europe. Location Europe. Methods We used a data set of 816,005 vegetation plots from the European Vegetation Archive (EVA). For each plot, we calculated the relative species richness of each plant family as the number of species belonging to that family divided by the total number of species. We mapped the relative species richness, averaged across all plots in 50 km × 50 km grid cells, for each family and broad habitat groups: forests, grasslands, scrub and wetlands. We also calculated the absolute species richness and the Shannon diversity index for each family. Results We produced 522 maps of mean relative species richness for a total of 152 vascular plant families occurring in forests, grasslands, scrub and wetlands. We found distinct spatial patterns for many combinations of families and habitat groups. The resulting series of 522 maps is freely available, both as images and GIS layers. Conclusions The distinct spatial patterns revealed in the maps suggest that the relative species richness of plant families at the community level reflects the evolutionary history of individual families. We believe that the maps and associated data can inspire further biogeographical and macroecological studies and strengthen the ongoing integration of phylogenetic, functional and taxonomic diversity concepts

Decoupled phylogenetic and functional diversity in European grasslands

The relationship between phylogenetic diversity (PD) and functional diversity (FD) is important for understanding the mechanisms of community assembly. The traditional view assumes a coupled (positively correlated) relationship between these two diversity measures, suggesting that competitive exclusion and environmental filtering are important drivers of both phylogenetic and functional structure of communities. In contrast, there is evidence that communities might deviate from this pattern, exhibiting either phylogenetic overdispersion connected with trait convergence (decoupled PD) or functional overdispersion connected with phylogenetic clustering (decoupled FD). In this study, we examined the relationship between PD and FD within vascular-plant communities in European grasslands, focusing on decoupled PD-FD patterns. We hypothesized that the decoupled patterns are connected with past or current environmental changes and are rarer in comparison with the coupled PD-FD pattern, reflecting long-term relatively stable environments. We used 81,484 plots (communities) of European dry, mesic, wet and alpine grasslands, containing 4,119 angiosperm species, and data on six functional traits relevant for different plant functions and habitats (plant height, leaf area, specific leaf area, leaf nitrogen content, seed mass and lateral spreading distance). Functional diversity was evaluated in two ways – as a single combined measure and as variability in each trait separately. We found various PD-FD patterns across different habitats, traits and regions, with the coupled pattern widespread but not universal. In many communities, we detected the tendency towards decoupled PD, likely caused by environmental filtering of phylogenetically diverse species pools. This was most pronounced in dry grasslands, and also in wet and alpine grasslands when FD based on plant height, leaf area or seed mass was considered. In contrast, the tendency towards decoupled FD was detected only in mesic and wet grasslands for leaf nitrogen content and lateral spreading distance, possibly due to competitive interactions among species interplaying with land-use history. Decoupled PD is relatively common in European grasslands, especially in mountainous and hilly areas of central and southern Europe and in parts of western Europe with a mild climate. This likely results from refugial effects that have preserved many distinct phylogenetic lineages, but their species are functionally similar due to environmental filters that affect the assembly of present-day grassland communities. We demonstrate that PD and FD may reflect different aspects of community structure and assembly mechanisms, and suggest that the phenomenon of decoupled PD and FD deserves more systematic study.</p