| human | Q5 |
| P269 | IdRef ID | 223738190 |
| P213 | ISNI | 0000000423154459 |
| P1207 | NUKAT ID | n2014005896 |
| P496 | ORCID iD | 0000-0002-2067-9108 |
| P3159 | UGentMemorialis professor ID | 000005796 |
| P214 | VIAF ID | 311376476 |
| P10832 | WorldCat Entities ID | E39PBJgH9FBhwFqrCxjtPcR7pP |
| P69 | educated at | Katholieke Universiteit Leuven | Q833670 |
| P108 | employer | Ghent University | Q1137665 |
| P734 | family name | Verheyen | Q15730702 |
| Verheyen | Q15730702 | ||
| Verheyen | Q15730702 | ||
| P6104 | maintained by WikiProject | WikiProject Invasion Biology | Q56241615 |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q56950221 | A million and more trees for science |
| Q57050636 | A model-based approach to studying changes in compositional heterogeneity |
| Q113873789 | A model-based scenario analysis of the impact of forest management and environmental change on the understorey of temperate forests in Europe |
| Q56978186 | A novel comparative research platform designed to determine the functional significance of tree species diversity in European forests |
| Q99576352 | A social-ecological framework and toolbox to help strengthening functional agrobiodiversity-supported ecosystem services at the landscape scale |
| Q57604631 | A spatially explicit empirical model on actual and potential ancient forest plant diversity in a fragmented landscape |
| Q112804327 | Above‐ and below‐ground complementarity rather than selection drive tree diversity–productivity relationships in European forests |
| Q49107984 | Acidification of forested podzols in North Belgium during the period 1950-2000. |
| Q59460515 | Adaptation of forest management to climate change as perceived by forest owners and managers in Belgium |
| Q112795679 | Afrotropical secondary forests exhibit fast diversity and functional recovery, but slow compositional and carbon recovery after shifting cultivation |
| Q57267253 | An experimental assessment of seed adhesivity on animal furs |
| Q57267278 | An integrated analysis of the effects of past land use on forest herb colonization at the landscape scale |
| Q57000362 | An intraspecific application of the leaf-height-seed ecology strategy scheme to forest herbs along a latitudinal gradient |
| Q57604641 | Application of the Ancient Forest Concept to Potential Natural Vegetation Mapping in Flanders, A Strongly Altered Landscape in Northern Belgium |
| Q57050673 | Assessment of the functional role of tree diversity: the multi-site FORBIO experiment |
| Q49033797 | Atmospheric nitrogen deposition on petals enhances seed quality of the forest herb Anemone nemorosa |
| Q36054825 | Bat and bird diversity along independent gradients of latitude and tree composition in European forests |
| Q57050580 | Beyond plant-soil feedbacks: mechanisms driving plant community shifts due to land-use legacies in post-agricultural forests |
| Q46304677 | Biodiversity and ecosystem functioning relations in European forests depend on environmental context |
| Q57050585 | Biodiversity as insurance for sapling survival in experimental tree plantations |
| Q57000427 | Biological Flora of the British Isles: Milium effusum |
| Q46242798 | Biotic and abiotic drivers of intraspecific trait variation within plant populations of three herbaceous plant species along a latitudinal gradient |
| Q110069177 | Biotic and abiotic drivers of soil microbial functions across tree diversity experiments |
| Q31058846 | Biotic homogenization can decrease landscape-scale forest multifunctionality |
| Q92963458 | Biotic predictors complement models of bat and bird responses to climate and tree diversity in European forests |
| Q108404200 | Body size and tree species composition determine variation in prey consumption in a forest‐inhabiting generalist predator |
| Q39558003 | Can complementarity in water use help to explain diversity-productivity relationships in experimental grassland plots? |
| Q57050677 | Can soil acidity and light help to explain tree species effects on forest herb layer performance in post-agricultural forests? |
| Q57050731 | Clear-felling effects on colonization rates of shade-tolerant forest herbs into a post-agricultural forest adjacent to ancient forest |
| Q112804520 | Climate affects neighbour‐induced changes in leaf chemical defences and tree diversity–herbivory relationships |
| Q57000224 | Climate warming and atmospheric deposition affect seed viability of common juniper (Juniperus communis) via their impact on the nutrient status of the plant |
| Q112818986 | Climatic conditions, not above- and belowground resource availability and uptake capacity, mediate tree diversity effects on productivity and stability |
| Q57000313 | Climatic control of forest herb seed banks along a latitudinal gradient |
| Q56950270 | Combining community resurvey data to advance global change research |
| Q126920429 | Combining multiple investigative approaches to unravel functional responses to global change in the understorey of temperate forests |
| Q49089028 | Comment on "In defense of plants as biomonitors of soil quality". |
| Q49157392 | Comparison of forest edge effects on throughfall deposition in different forest types |
| Q114147024 | Competition mediates understorey species range shifts under climate change |
| Q57000239 | Complementary distribution patterns of arthropod detritivores (woodlice and millipedes) along forest edge-to-interior gradients |
| Q114224994 | Context matters: the landscape matrix determines the population genetic structure of temperate forest herbs across Europe |
| Q46260539 | Continental mapping of forest ecosystem functions reveals a high but unrealised potential for forest multifunctionality |
| Q40240195 | Contributing factors in foliar uptake of dissolved inorganic nitrogen at leaf level. |
| Q30986763 | Contributions of a global network of tree diversity experiments to sustainable forest plantations |
| Q57267159 | Coppice management effects on experimentally established populations of three herbaceous layer woodland species |
| Q48158267 | Correction to Multilayered Modeling of Particulate Matter Removal by a Growing Forest over Time, From Plant Surface Deposition to Washoff via Rainfall |
| Q57249421 | Correction: Schelfhout, S.; et al. Tree Species Identity Shapes Earthworm Communities. Forests 2017, 8, 85 |
| Q57000365 | Cumulative nitrogen input drives species loss in terrestrial ecosystems |
| Q124788437 | Declining potential nectar production of the herb layer in temperate forests under global change |
| Q59599538 | Desiccation resistance determines distribution of woodlice along forest edge-to-interior gradients |
| Q126920421 | Different effects of warming treatments in forests versus hedgerows on the understorey plant Geum urbanum |
| Q57267268 | Differential environmental response of plant functional types in hedgerow habitats |
| Q110970613 | Directional turnover towards larger‐ranged plants over time and across habitats |
| Q57050617 | Disentangling dispersal from phylogeny in the colonization capacity of forest understorey plants |
| Q56775198 | Disentangling relationships between habitat conditions, disturbance history, plant diversity, and American black cherry (Prunus serotina Ehrh.) invasion in a European temperate forest |
| Q113799739 | Disentangling the interrelated abiotic and biotic pathways linking landscape composition and crop production |
| Q57050622 | Disentangling tree species identity and richness effects on the herb layer: first results from a German tree diversity experiment |
| Q58075122 | Distinct growth responses to drought for oak and beech in temperate mixed forests |
| Q57050710 | Distinguishing between turnover and nestedness in the quantification of biotic homogenization |
| Q115808416 | Divergent roles of herbivory in eutrophying forests |
| Q57050774 | Diverging effects of overstorey conversion scenarios on the understorey vegetation in a former coppice-with-standards forest |
| Q36016158 | Diversifying forest communities may change Lyme disease risk: extra dimension to the dilution effect in Europe |
| Q57267150 | Does Prunus serotina act as an aggressive invader in areas with a low propagule pressure? |
| Q57050599 | Does neighbourhood tree diversity affect the crown arthropod community in saplings? |
| Q57262784 | Dominance of individual plant species is more important than diversity in explaining plant biomass in the forest understorey |
| Q112803037 | Drivers of above‐ground understorey biomass and nutrient stocks in temperate deciduous forests |
| Q103024632 | Drivers of carbon stocks in forest edges across Europe |
| Q57249431 | Drivers of earthworm incidence and abundance across European forests |
| Q35714874 | Drivers of temporal changes in temperate forest plant diversity vary across spatial scales |
| Q57000338 | Driving factors behind the eutrophication signal in understorey plant communities of deciduous temperate forests |
| Q96687983 | Earlier onset of flowering and increased reproductive allocation of an annual invasive plant in the north of its novel range |
| Q57000399 | Early Trajectories of Spontaneous Vegetation Recovery after Intensive Agricultural Land Use |
| Q56937613 | Early stage litter decomposition across biomes |
| Q57000321 | Ecological niche shifts of understorey plants along a latitudinal gradient of temperate forests in north-western Europe |
| Q56950209 | Ecological restoration efforts in tropical rural landscapes: Challenges and policy implications in a highly degraded region |
| Q57000245 | Ecosystem Services from Small Forest Patches in Agricultural Landscapes |
| Q57050648 | Ecosystem services of mixed species forest stands and monocultures: comparing practitioners' and scientists' perceptions with formal scientific knowledge |
| Q49070617 | Edge effects in temperate forests subjected to high nitrogen deposition. |
| Q40410627 | Edge effects on N2O, NO and CH4 fluxes in two temperate forests |
| Q57050545 | Effects of Mineral Soil and Forest Floor on the Regeneration of Pedunculate Oak, Beech and Red Oak |
| Q60409427 | Effects of charcoal hearth soil on forest regeneration: Evidence from a two-year experiment on tree seedlings |
| Q111172410 | Effects of climate change and horticultural use on the spread of naturalized alien garden plants in Europe |
| Q57265017 | Effects of drought legacy and tree species admixing on bacterial growth and respiration in a young forest soil upon drying and rewetting |
| Q57000296 | Effects of enhanced nitrogen inputs and climate warming on a forest understorey plant assessed by transplant experiments along a latitudinal gradient |
| Q56784099 | Effects of landscape structure on the invasive spread of black cherry Prunus serotina in an agricultural landscape in Flanders, Belgium |
| Q31112021 | Effects of two contrasting hemiparasitic plant species on biomass production and nitrogen availability |
| Q114083302 | Emerging stability of forest productivity by mixing two species buffers temperature destabilizing effect |
| Q57802958 | Environmental drivers interactively affect individual tree growth across temperate European forests |
| Q60400090 | Environmental drivers interactively affect individual tree growth across temperate European forests |
| Q40066140 | Environmental drivers of Ixodes ricinus abundance in forest fragments of rural European landscapes |
| Q46830849 | Environmental drivers of ectomycorrhizal communities in Europe's temperate oak forests |
| Q31058002 | Environmental impact assessment and monetary ecosystem service valuation of an ecosystem under different future environmental change and management scenarios; a case study of a Scots pine forest |
| Q56771943 | Environmental limitation contributes to the differential colonization capacity of two forest herbs |
| Q57267164 | Epizoochory by large herbivores: merging data with models |
| Q59459538 | Erratum to: Adaptation of forest management to climate change as perceived by forest owners and managers in Belgium |
| Q60339741 | EuMIXFOR empirical forest mensuration and ring width data from pure and mixed stands of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.) through Europe |
| Q57536071 | European Mixed Forests: definition and research perspectives |
| Q125465311 | Evaluating plant lineage losses and gains in temperate forest understories: a phylogenetic perspective on climate change and nitrogen deposition |
| Q115596103 | Evaluating structural and compositional canopy characteristics to predict the light‐demand signature of the forest understorey in mixed, semi‐natural temperate forests |
| Q56950245 | Evaluating the robustness of three ring-width measurement methods for growth release reconstruction |
| Q57000374 | Experimental assessment of ecological restoration options for compacted forest soils |
| Q57267219 | Experimental assessment of plant seed retention times in fur of cattle and horse |
| Q57000342 | Experimental assessment of the survival and performance of forest herbs transplanted beyond their range limit |
| Q108404330 | Exploring the faecal microbiome of the Eurasian nuthatch (Sitta europaea) |
| Q33239221 | Extinction debt of forest plants persists for more than a century following habitat fragmentation |
| Q56767911 | Factors affecting radial growth of the invasive Prunus serotina in pine plantations in Flanders |
| Q107557050 | For the sake of resilience and multifunctionality, let's diversify planted forests! |
| Q106291964 | Forest edges reduce slug (but not snail) activity-density across Western Europe |
| Q46575675 | Forest floor leachate fluxes under six different tree species on a metal contaminated site |
| Q92359076 | Forest fragmentation modulates effects of tree species richness and composition on ecosystem multifunctionality |
| Q57000301 | Forest herbs show species-specific responses to variation in light regime on sites with contrasting soil acidity: An experiment mimicking forest conversion scenarios |
| Q94685299 | Forest microclimate dynamics drive plant responses to warming |
| Q115596079 | Forest structure and composition alleviate human thermal stress |
| Q109416024 | Forest understorey communities respond strongly to light in interaction with forest structure, but not to microclimate warming |
| Q112794917 | Forest understorey plant responses to long‐term experimental warming, light and nitrogen addition |
| Q60409454 | Former charcoal kiln platforms as microhabitats affecting understorey vegetation in Mediterranean forests |
| Q57000379 | Former land use affects the nitrogen and phosphorus concentrations and biomass of forest herbs |
| Q49041057 | Four decades of post-agricultural forest development have caused major redistributions of soil phosphorus fractions |
| Q62923440 | Functional Composition of Tree Communities Changed Topsoil Properties in an Old Experimental Tropical Plantation |
| Q56950192 | Functional trait variation of forest understorey plant communities across Europe |
| Q57267165 | Garden plants get a head start on climate change |
| Q28740282 | Genetic structure and seed-mediated dispersal rates of an endangered shrub in a fragmented landscape: a case study for Juniperus communis in northwestern Europe |
| Q57267171 | Germination ecology of the holoparasite Cuscuta epithymum |
| Q57006123 | Germination requirements and seed mass of slow- and fast- colonizing temperate forest herbs along a latitudinal gradient |
| Q64214087 | Global buffering of temperatures under forest canopies |
| Q31019176 | Global environmental change effects on ecosystems: the importance of land-use legacies |
| Q47177968 | Global environmental change effects on plant community composition trajectories depend upon management legacies. |
| Q35027576 | Global meta-analysis reveals no net change in local-scale plant biodiversity over time |
| Q57536063 | Growth and yield of mixed versus pure stands of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.) analysed along a productivity gradient through Europe |
| Q57050737 | Habitat preferences of European NightjarsCaprimulgus europaeusin forests on sandy soils |
| Q47557177 | Habitat properties are key drivers of Borrelia burgdorferi (s.l.) prevalence in Ixodes ricinus populations of deciduous forest fragments |
| Q112795788 | Hedging against biodiversity loss: Forest herbs’ performance in hedgerows across temperate Europe |
| Q57267124 | Hemiparasitic litter additions alter gross nitrogen turnover in temperate semi-natural grassland soils |
| Q57050764 | Herb layer changes (1954-2000) related to the conversion of coppice-with-standards forest and soil acidification |
| Q58827695 | Herbaceous plant community structure of ancient and recent forests in two contrasting forest types |
| Q57267149 | Hidden in the host – Unexpected vegetative hibernation of the holoparasite Cuscuta epithymum (L.) L. and its implications for population persistence |
| Q112803681 | High ecosystem service delivery potential of small woodlands in agricultural landscapes |
| Q57267314 | High-resolution continuous soil classification using morphological soil profile descriptions |
| Q59222259 | Hints for alternative stable states from long-term vegetation dynamics in an unmanaged heathland |
| Q59612232 | How are biodiversity and dispersal of species affected by the management of roadsides? A systematic map |
| Q59476375 | How are biodiversity and dispersal of species affected by the management of roadsides? A systematic map protocol |
| Q90887739 | How do trees respond to species mixing in experimental compared to observational studies? |
| Q57236133 | How does neighbourhood tree species composition affect growth characteristics of oak saplings? |
| Q60532958 | How does roadside vegetation management affect the diversity of vascular plants and invertebrates? A systematic review |
| Q59611306 | How does roadside vegetation management affect the diversity of vascular plants and invertebrates? A systematic review protocol |
| Q47115123 | How tree species identity and diversity affect light transmittance to the understory in mature temperate forests |
| Q62552230 | Identifying the tree species compositions that maximize ecosystem functioning in European forests |
| Q57236134 | Identity rather than richness drives local neighbourhood species composition effects on oak sapling growth in a young forest |
| Q59160563 | Impact of an invasive alien plant on litter decomposition along a latitudinal gradient |
| Q56774454 | Impact of avian frugivores on dispersal and recruitment of the invasive Prunus serotina in an agricultural landscape |
| Q57267161 | Impact of hemiparasitic Rhinanthus angustifolius and R. minor on nitrogen availability in grasslands |
| Q60254655 | Importance of forest fragments as pollinator habitat varies with season and guild |
| Q97593374 | Importance of overstorey attributes for understorey litter production and nutrient cycling in European forests |
| Q59222255 | Indirect effects of land-use legacies determine tree colonization patterns in abandoned heathland |
| Q89936261 | Individualistic responses of forest herb traits to environmental change |
| Q57050692 | Influence of canopy budget model approaches on atmospheric deposition estimates to forests |
| Q57267232 | Intensive management fails to promote recruitment in the last large population of Juniperus communis (L.) in Flanders (Belgium) |
| Q57000383 | Interregional variation in the floristic recovery of post-agricultural forests |
| Q27321789 | Jack-of-all-trades effects drive biodiversity-ecosystem multifunctionality relationships in European forests |
| Q60339723 | Knowledge gaps about mixed forests: What do European forest managers want to know and what answers can science provide? |
| Q57267197 | Landscape factors and regional differences in recovery rates of herb layer richness in Flanders (Belgium) |
| Q112799706 | Land‐use legacies predispose the response of trees to drought in restored forests |
| Q57267241 | Large herbivores as mobile links between isolated nature reserves through adhesive seed dispersal |
| Q57000327 | Latitudinal gradients as natural laboratories to infer species' responses to temperature |
| Q56332777 | Latitudinal variation of life-history traits of an exotic and a native impatiens species in Europe |
| Q128154635 | Leaf isotopes reveal tree diversity effects on the functional responses to the pan‐European 2018 summer drought |
| Q126920432 | Leaf trait variation in grassland plant species in response to soil phosphorus |
| Q57267187 | Legacies of the past in the present-day forest biodiversity: a review of past land-use effects on forest plant species composition and diversity |
| Q57267193 | Legacies of the past in the present-day forest biodiversity: a review of past land-use effects on forest plant species composition and diversity |
| Q57267179 | Life-history traits are correlated with geographical distribution patterns of western European forest herb species |
| Q39717828 | Light accelerates plant responses to warming |
| Q91771748 | Light and warming drive forest understorey community development in different environments |
| Q112803020 | Light availability and land‐use history drive biodiversity and functional changes in forest herb layer communities |
| Q57267143 | Limited by the host: Host age hampers establishment of holoparasite Cuscuta epithymum |
| Q125476325 | Limited effects of population age on the genetic structure of spatially isolated forest herb populations in temperate Europe |
| Q59599536 | Linking macrodetritivore distribution to desiccation resistance in small forest fragments embedded in agricultural landscapes in Europe |
| Q112823476 | Litter quality, land-use history, and nitrogen deposition effects on topsoil conditions across European temperate deciduous forests |
| Q57267177 | Local and regional factors affecting the distribution of the endangered holoparasite Cuscuta epithymum in heathlands |
| Q57050721 | Local habitat and landscape affect Ixodes ricinus tick abundances in forests on poor, sandy soils |
| Q57050560 | Local neighbourhood effects on sapling growth in a young experimental forest |
| Q60722011 | Long-term dynamics in a planted conifer forest with spontaneous ingrowth of broad-leaved trees |
| Q57267200 | Long-term dynamics of the hemiparasiteRhinanthus angustifoliusand its relationship with vegetation structure |
| Q56763291 | Long-term scenarios of the invasive black cherry in pine-oak forest: Impact of regeneration success |
| Q57267168 | Long-term seed bank dynamics in a temperate forest under conversion from coppice-with-standards to high forest management |
| Q57263554 | Low probability of a dilution effect for Lyme borreliosis in Belgian forests |
| Q57050768 | Low recruitment across life stages partly accounts for the slow colonization of forest herbs |
| Q57267272 | METAPOPULATION DYNAMICS IN CHANGING LANDSCAPES: A NEW SPATIALLY REALISTIC MODEL FOR FOREST PLANTS |
| Q57050780 | Management driven changes (1967–2005) in soil acidity and the understorey plant community following conversion of a coppice-with-standards forest |
| Q60537365 | Maternal temperature during seed maturation affects seed germination and timing of bud set in seedlings of European black poplar |
| Q37686402 | Melting pot of tick-borne zoonoses: the European hedgehog contributes to the maintenance of various tick-borne diseases in natural cycles urban and suburban areas |
| Q57267216 | Meta-analysis of standing crop reduction byRhinanthus spp. and its effect on vegetation structure |
| Q46918847 | Metal and nutrient dynamics in decomposing tree litter on a metal contaminated site |
| Q57267155 | Metapopulation viability of an endangered holoparasitic plant in a dynamic landscape |
| Q100457444 | Microclimate limits thermal behaviour favourable to disease control in a nocturnal amphibian |
| Q30685482 | Microclimate moderates plant responses to macroclimate warming |
| Q109416003 | Microclimatic edge-to-interior gradients of European deciduous forests |
| Q57031378 | Mitigating the impact of microbial pressure on great (Parus major) and blue (Cyanistes caeruleus) tit hatching success through maternal immune investment |
| Q57050610 | Mixing effects on litter decomposition rates in a young tree diversity experiment |
| Q57536061 | Mixing of Scots pine ( Pinus sylvestris L.) and European beech ( Fagus sylvatica L.) enhances structural heterogeneity, and the effect increases with water availability |
| Q112803591 | Mixing of tree species is especially beneficial for biodiversity in fragmented landscapes, without compromising forest functioning |
| Q52328609 | Modelling understorey dynamics in temperate forests under global change-Challenges and perspectives. |
| Q88945741 | Monitoring the Impact of Hedgerows and Grass Strips on the Performance of Multiple Ecosystem Service Indicators |
| Q39142915 | Multilayered modeling of particulate matter removal by a growing forest over time, from plant surface deposition to washoff via rainfall |
| Q112799278 | Multiscale drivers of carabid beetle (Coleoptera: Carabidae) assemblages in small European woodlands |
| Q129961714 | Mycorrhizal associations modify tree diversity−productivity relationships across experimental tree plantations |
| Q100692945 | NITROGEN FLUXES IN THROUGHFALL AND LITTERFALL IN TWO NOTHOFAGUS FORESTS IN SOUTHERN CHILE |
| Q49031663 | Nitrogen saturation and net ecosystem production |
| Q64254350 | No genetic erosion after five generations for Impatiens glandulifera populations across the invaded range in Europe |
| Q56755156 | Nutrient input from hemiparasitic litter favors plant species with a fast-growth strategy |
| Q60537366 | Observer and relocation errors matter in resurveys of historical vegetation plots |
| Q57000352 | On the use of weather data in ecological studies along altitudinal and latitudinal gradients |
| Q108404254 | Overstorey composition shapes across‐trophic level community relationships in deciduous forest regardless of fragmentation context |
| Q56950251 | P-removal for restoration of Nardus grasslands on former agricultural land: cutting traditions |
| Q57000277 | Patterns of phenotypic trait variation in two temperate forest herbs along a broad climatic gradient |
| Q57267292 | Permeability of ancient forest edges for weedy plant species invasion |
| Q29999147 | Persistent changes in forest vegetation and seed bank 1,600 years after human occupation |
| Q59222234 | Persistent land-use legacies increase small-scale diversity and strengthen vegetation–soil relationships on an unmanaged heathland |
| Q89006774 | Phosphorus mining efficiency declines with decreasing soil P concentration and varies across crop species |
| Q36866869 | Phytoextraction of metals from soils: how far from practice? |
| Q60537367 | Plant and soil microbe responses to light, warming and nitrogen addition in a temperate forest |
| Q115408509 | Plant diversity in hedgerows and road verges across Europe |
| Q91998217 | Plant functional trait response to environmental drivers across European temperate forest understorey communities |
| Q30725756 | Plant movements and climate warming: intraspecific variation in growth responses to nonlocal soils |
| Q91755976 | Plant species identity and soil characteristics determine rhizosphere soil bacteria community composition in European temperate forests |
| Q57267263 | Plant species loss in an urban area (Turnhout, Belgium) from 1880 to 1999 and its environmental determinants |
| Q91120087 | Plant-soil feedbacks of forest understorey plants transplanted in nonlocal soils along a latitudinal gradient |
| Q49108966 | Plasticity in response to phosphorus and light availability in four forest herbs |
| Q57267257 | Population structure and adult plant performance of forest herbs in three contrasting habitats |
| Q57267291 | Possible effects of habitat fragmentation and climate change on the range of forest plant species |
| Q60254874 | Potential of Short Rotation Coppice plantations to reinforce functional biodiversity in agricultural landscapes |
| Q57236135 | Productivity, stand dynamics and the selection effect in a mixed willow clone short rotation coppice plantation |
| Q53820024 | Promoting biodiversity values of small forest patches in agricultural landscapes: Ecological drivers and social demand. |
| Q56767810 | Prunus serotina unleashed: invader dominance after 70 years of forest development |
| Q107559770 | Quantifying establishment limitations during the ecological restoration of species-rich Nardus grassland |
| Q35032955 | Quantifying the environmental impact of an integrated human/industrial-natural system using life cycle assessment; a case study on a forest and wood processing chain |
| Q107584681 | RHINANTHUS: AN EFFECTIVE TOOL IN REDUCING BIOMASS OF ROAD VERGES? AN EXPERIMENT ALONG TWO MOTORWAYS |
| Q106350410 | Rapid thermophilization of understorey plant communities in a 9 year‐long temperate forest experiment |
| Q125503281 | ReSurveyEurope: A database of resurveyed vegetation plots in Europe |
| Q57267259 | Recruitment and growth of herb-layer species with different colonizing capacities in ancient and recent forests |
| Q91874891 | Replacements of small- by large-ranged species scale up to diversity loss in Europe's temperate forest biome |
| Q57267281 | Response of forest plant species to land-use change: a life-history trait-based approach |
| Q103000285 | Response to Comment on "Forest microclimate dynamics drive plant responses to warming" |
| Q104281773 | Response to Comment on "Forest microclimate dynamics drive plant responses to warming" |
| Q56950202 | Responses of competitive understorey species to spatial environmental gradients inaccurately explain temporal changes |
| Q112833099 | Restoring tropical forest composition is more difficult, but recovering tree-cover is faster, when neighbouring forests are young |
| Q59330176 | Role of mustelids in the life-cycle of ixodid ticks and transmission cycles of four tick-borne pathogens |
| Q108404180 | Salamander loss alters litter decomposition dynamics |
| Q92187238 | Seasonal drivers of understorey temperature buffering in temperate deciduous forests across Europe |
| Q57267136 | Seed banking in ancient forest species: why total sampled area really matters |
| Q57267139 | Seed banks of temperate deciduous forests during secondary succession |
| Q109418785 | Sensitivity to habitat fragmentation across European landscapes in three temperate forest herbs |
| Q49138758 | Shrub clearing adversely affects the abundance of Ixodes ricinus ticks |
| Q90315127 | Skin mucosome activity as an indicator of Batrachochytrium salamandrivorans susceptibility in salamanders |
| Q64031982 | Small forest patches as pollinator habitat: oases in an agricultural desert? |
| Q112799271 | Small scale environmental variation modulates plant defence syndromes of understorey plants in deciduous forests of Europe |
| Q57267142 | Small-scale seed-bank patterns in a forest soil |
| Q126920433 | Soil legacies of tree species richness in a young plantation do not modulate tree seedling response to watering regime |
| Q56950229 | Soil properties and neighbouring forest cover affect above-ground biomass and functional composition during tropical forest restoration |
| Q49097389 | Spatial variability and temporal stability of throughfall deposition under beech (Fagus sylvatica L.) in relationship to canopy structure |
| Q57267306 | Spatio-temporal colonization patterns of forest plant species in a mixed deciduous forest |
| Q113792337 | Species distribution models and a 60‐year‐old transplant experiment reveal inhibited forest plant range shifts under climate change |
| Q33574649 | Stronger diversity effects with increased environmental stress: A study of multitrophic interactions between oak, powdery mildew and ladybirds |
| Q56937636 | Synthesis and future research directions linking tree diversity to growth, survival, and damage in a global network of tree diversity experiments |
| Q107584732 | THE IMPORTANCE OF ARTEFACTS OF ANCIENT LAND USE ON PLANT COMMUNITIES IN MEERDAAL FOREST, BELGIUM |
| Q92348862 | TRY plant trait database - enhanced coverage and open access |
| Q112802853 | Taxonomic, phylogenetic and functional diversity of understorey plants respond differently to environmental conditions in European forest edges |
| Q57000330 | Temporal changes in forest plant communities at different site types |
| Q39570681 | Temporal variation and high-resolution spatial heterogeneity in soil CO2 efflux in a short-rotation tree plantation |
| Q57604636 | The analysis of spatio-temporal forest changes (1775–2000) in Flanders (northern Belgium) indicates habitat-specific levels of fragmentation and area loss |
| Q112799745 | The combined effects of climate and canopy cover changes on understorey plants of the Hyrcanian forest biodiversity hotspot in northern Iran |
| Q57000289 | The contribution of patch-scale conditions is greater than that of macroclimate in explaining local plant diversity in fragmented forests across Europe |
| Q57050746 | The effect of air pollution and other environmental stressors on leaf fluctuating asymmetry and specific leaf area of Salix alba L |
| Q126920434 | The effect of forest structural complexity on tick-borne pathogens in questing ticks and small mammals |
| Q36880784 | The effect of forest type on throughfall deposition and seepage flux: a review |
| Q57000292 | The effects of hemiparasitic plant removal on community structure and seedling establishment in semi-natural grasslands |
| Q57050665 | The effects of local neighbourhood diversity on pest and disease damage of trees in a young experimental forest |
| Q49067900 | The effects of sampling method and vegetation type on the estimated abundance of Ixodes ricinus ticks in forests |
| Q91845404 | The functional role of temperate forest understorey vegetation in a changing world |
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