| sPlot - A new tool for global vegetation analyses |
35 |
| Observer and relocation errors matter in resurveys of historical vegetation plots |
17 |
| Make it simpler: Alien species decrease functional diversity of coastal plant communities |
15 |
| The symmetry of competitive interactions in mixed Norway spruce, silver fir and European beech forests |
9 |
| Changes in vegetation structure and fuel characteristics along post-fire succession promote alternative stable states and positive fire-vegetation feedbacks |
9 |
| Effects of natural and anthropogenic drivers on land-cover change and treeline dynamics in the Apennines (Italy) |
9 |
| GRIMP: A machine-learning method for improving groups of discriminating species in expert systems for vegetation classification |
9 |
| Which results of the standard test for community-weighted mean approach are too optimistic? |
8 |
| Requirements of plant species are linked to area and determine species pool and richness on small islands |
7 |
| Interactive effects of past land use and recent forest management on the understorey community in temperate oak forests in South Sweden |
7 |
| Responses of peatland vegetation to 15-year water level drawdown as mediated by fertility level |
7 |
| Patterns of long-term vegetation change vary between different types of semi-natural grasslands in Western and Central Europe |
7 |
| Long-term vegetation changes of treeless heath communities in northern Fennoscandia: Links to climate change trends and reindeer grazing |
7 |
| Invasive species differ in key functional traits from native and non-invasive alien plant species |
7 |
| Drivers of the beta diversity of aquatic plant communities along a latitudinal gradient in southern Brazilian coastal ponds |
6 |
| Global database of plants with root-symbiotic nitrogen fixation: NodDB |
6 |
| Salt marsh migration into salinized agricultural fields: A novel assembly of plant communities |
6 |
| Environment and dispersal influence changes in species composition at different scales in woody plants of the Western Ghats, India |
6 |
| It's a long way to the top: Plant species diversity in the transition from managed to old-growth forests |
6 |
| How cyclical and predictable are Central European temperate forest dynamics in terms of development phases? |
6 |
| Dominance of individual plant species is more important than diversity in explaining plant biomass in the forest understorey |
6 |
| The role of climate, forest fires and human population size in Holocene vegetation dynamics in Fennoscandia |
6 |
| Invasive acacias differ from native dune species in the hyperspectral/biochemical trait space |
6 |
| Will I stay or will I go? Plant species-specific response and tolerance to high land-use intensity in temperate grassland ecosystems |
6 |
| Accidental epiphytism in the Harz Mountains, Central Europe |
6 |
| New insights into plants co-existence in species-rich communities: The pollination interaction perspective |
6 |
| Interactions between abiotic gradients determine functional and phylogenetic diversity patterns in Mediterranean-type climate mountains in the Andes |
5 |
| A novel method to predict dark diversity using unconstrained ordination analysis |
5 |
| Geese are overlooked dispersal vectors for vascular plants in archipelago environments |
5 |
| Long-term dynamics of the East European forest-steppe ecotone |
5 |
| Environmental filtering limits functional diversity during succession in a seasonally wet tropical secondary forest |
5 |
| Holocene vegetation history of the Jeseniky Mts: Deepening elevational contrast in pollen assemblages since late prehistory |
5 |
| Long-term changes in regional vegetation cover along the west coast of southern Norway: The importance of human impact |
5 |
| Legacy of historical litter raking in temperate forest plant communities |
5 |
| Environmental filters shaping angiosperm tree assembly along climatic and geographic gradients |
5 |
| Water source partitioning among plant functional types in a semi-arid dune ecosystem |
5 |
| Cushion and shrub ecosystem engineers contribute differently to diversity and functions in alpine ecosystems |
5 |
| Interactive effects of climate and topography on soil salinity and vegetation zonation in North-African continental saline depressions |
4 |
| Hierarchical species distribution models in support of vegetation conservation at the landscape scale |
4 |
| Hedgerow age affects the species richness of herbaceous forest plants |
4 |
| Species interactions weakly modify climate-induced tree co-occurrence patterns |
4 |
| Temporal niche differentiation among species changes with habitat productivity and light conditions |
4 |
| Carbon forms, nutrients and water velocity filter hydrophyte and riverbank species differently: A trait-based study |
4 |
| Role of climate and herbivory on native and alien conifer seedling recruitment at and above the Fennoscandian tree line |
4 |
| Effects of connectivity on animal-dispersed forest plant communities in agriculture-dominated landscapes |
4 |
| Impacts of an invasive plant on primary production: Testing a functional trait-based framework with a greenhouse experiment |
4 |
| Boreal bog plant communities along a water table gradient differ in their standing biomass but not their biomass production |
4 |
| Nitrogen uptake and biomass resprouting show contrasting relationships with resource acquisitive and conservative plant traits |
4 |
| Proportion of fine roots, but not plant biomass allocation below ground, increases with elevation in arctic tundra |
4 |
| Functional diversity differently shapes growth resilience to drought for co-existing pine species |
4 |
