| Q58195630 | A comparison of Guibourtia copallifera Benn. stands in South West Burkina Faso-community structure and regeneration |
| Q57020319 | A framework for quantifying the magnitude and variability of community responses to global change drivers |
| Q33591170 | A global comparison of grassland biomass responses to CO2 and nitrogen enrichment |
| Q36345482 | A gradient of nutrient enrichment reveals nonlinear impacts of fertilization on Arctic plant diversity and ecosystem function |
| Q89689378 | A mechanism of expansion: Arctic deciduous shrubs capitalize on warming-induced nutrient availability |
| Q92460271 | A multitrophic perspective on biodiversity-ecosystem functioning research |
| Q35968010 | A novel soil manganese mechanism drives plant species loss with increased nitrogen deposition in a temperate steppe |
| Q57006609 | A phylogenetically-informed trait-based analysis of range change in the vascular plant flora of Britain |
| Q33724350 | A test of the niche dimension hypothesis in an arid annual grassland |
| Q58827534 | A trait-based analysis of the role of phosphorus vs. nitrogen enrichment in plant species loss across North-west European grasslands |
| Q39156244 | Above- and belowground responses to nitrogen addition in a Chihuahuan Desert grassland. |
| Q35626463 | Abundance of common species, not species richness, drives delivery of a real-world ecosystem service |
| Q35630160 | Abundance- and functional-based mechanisms of plant diversity loss with fertilization in the presence and absence of herbivores. |
| Q56461836 | Accidental experiments: ecological and evolutionary insights and opportunities derived from global change |
| Q31041800 | Altered rainfall patterns increase forb abundance and richness in native tallgrass prairie. |
| Q35138322 | Ammonium as a driving force of plant diversity and ecosystem functioning: observations based on 5 years' manipulation of N dose and form in a Mediterranean ecosystem |
| Q33664058 | An African grassland responds similarly to long-term fertilization to the Park Grass experiment |
| Q89766869 | An experimental test of the area-heterogeneity tradeoff |
| Q35600702 | Assembly of root-associated bacteria communities: interactions between abiotic and biotic factors |
| Q92435923 | Assessing the utility of conserving evolutionary history |
| Q98164352 | Below-ground herbivory mitigates biomass loss from above-ground herbivory of nitrogen fertilized plants |
| Q36370924 | Biogeochemistry drives diversity in the prokaryotes, fungi, and invertebrates of a Panama forest. |
| Q51720628 | Biotic homogenization and changes in species diversity across human-modified ecosystems. |
| Q51652270 | CO2, nitrogen, and diversity differentially affect seed production of prairie plants. |
| Q30394482 | Calcium induces long-term legacy effects in a subalpine ecosystem |
| Q57007770 | Can functional traits predict plant community response to global change? |
| Q56526807 | Central European plant species from more productive habitats are more invasive at a global scale |
| Q28598076 | Changes in litter quality induced by nutrient addition alter litter decomposition in an alpine meadow on the Qinghai-Tibet Plateau |
| Q57068245 | Changes in plant community composition, not diversity, during a decade of nitrogen and phosphorus additions drive above-ground productivity in a tallgrass prairie |
| Q34016572 | Changes in plant species richness induce functional shifts in soil nematode communities in experimental grassland |
| Q36341666 | Chronic N enrichment and drought alter plant cover and community composition in a Mediterranean-type semi-arid shrubland. |
| Q63388448 | Chronic fertilization and irrigation gradually and increasingly restructure grassland communities |
| Q41228339 | Climate and air pollution impacts on habitat suitability of Austrian forest ecosystems |
| Q30939960 | Climate and soil attributes determine plant species turnover in global drylands. |
| Q30315218 | Climate modifies response of non-native and native species richness to nutrient enrichment. |
| Q33626914 | Climate warming and biomass accumulation of terrestrial plants: a meta-analysis. |
| Q90234455 | Clonality-dependent dynamic change of plant community in temperate grasslands under nitrogen enrichment |
| Q56439410 | Community disassembly and invasion of remnant native grasslands under fluctuating resource supply |
| Q57187402 | Community traitscape of foliar nitrogen isotopes reveals N availability patterns in a tallgrass prairie |
| Q35896308 | Comparative metagenomic, phylogenetic and physiological analyses of soil microbial communities across nitrogen gradients |
| Q57269834 | Comparing the responses of bryophytes and short-statured vascular plants to climate shifts and eutrophication |
| Q43096866 | Competition and soil resource environment alter plant-soil feedbacks for native and exotic grasses |
| Q35234254 | Competitive exclusion, beta diversity, and deterministic vs. stochastic drivers of community assembly |
| Q56469539 | Competitive interaction between the exotic plant Rhus typhina L. and the native tree Quercus acutissima Carr. in Northern China under different soil N:P ratios |
| Q57007981 | Complementarity as a mechanism of coexistence between functional groups of grasses |
| Q92357005 | Composition, Diversity and Functional Analysis of the Modern Microbiome of the Middle Triassic Cava Superiore Beds (Monte San Giorgio, Switzerland) |
| Q35976794 | Conditional vulnerability of plant diversity to atmospheric nitrogen deposition across the United States |
| Q46139022 | Consistency and sensitivity of stream periphyton community structural and functional responses to nutrient enrichment |
| Q51607816 | Consistent effects of nitrogen fertilization on soil bacterial communities in contrasting systems. |
| Q28607736 | Consistent responses of soil microbial communities to elevated nutrient inputs in grasslands across the globe |
| Q33288347 | Consumer versus resource control of producer diversity depends on ecosystem type and producer community structure |
| Q90710524 | Contrasting patterns of functional diversity in coffee root fungal communities associated with organic and conventionally-managed fields |
| Q56979902 | Contrasting relationships between precipitation and species richness in space and time |
| Q35961774 | Contrasting the effects of environment, dispersal and biotic interactions to explain the distribution of invasive plants in alpine communities |
| Q91528834 | Critical transition of soil bacterial diversity and composition triggered by nitrogen enrichment |
| Q46266588 | Cumulative and partially recoverable impacts of nitrogen addition on a temperate steppe. |
| Q57000365 | Cumulative nitrogen input drives species loss in terrestrial ecosystems |
| Q56942843 | Decoupling the direct and indirect effects of nitrogen deposition on ecosystem function |
| Q34044269 | Delivery of crop pollination services is an insufficient argument for wild pollinator conservation |
| Q38903882 | Development of a diverse epiphyte community in response to phosphorus fertilization |
| Q56520212 | Differences in nitrogen use strategies between native and exotic tree species: predicting impacts on invaded ecosystems |
| Q51348082 | Different inter-annual responses to availability and form of nitrogen explain species coexistence in an alpine meadow community after release from grazing. |
| Q89814024 | Direct and indirect effects of temperature and precipitation on alpine seed banks in the Tibetan Plateau |
| Q57018407 | Dispersal-driven homogenization of wetland vegetation revealed from local contributions to β-diversity |
| Q33309765 | Diversification rates increase with population size and resource concentration in an unstructured habitat |
| Q51566291 | Diversity-dependent stability under mowing and nutrient addition: evidence from a 7-year grassland experiment. |
| Q28541229 | Does land-use intensification decrease plant phylogenetic diversity in local grasslands? |
| Q96822078 | Does plant community plasticity mediate microbial homeostasis? |
| Q57262183 | Drivers of Variation in Aboveground Net Primary Productivity and Plant Community Composition Differ Across a Broad Precipitation Gradient |
| Q30959210 | Ecology. Biodiversity under global change |
| Q57007988 | Ecosystem responses to water and nitrogen amendment in a California grassland |
| Q64281171 | Effect of breeding on nitrogen use efficiency-associated traits in oilseed rape |
| Q28743447 | Effects of elevated CO2 and N addition on growth and N2 fixation of a legume subshrub (Caragana microphylla Lam.) in temperate grassland in China |
| Q38927748 | Effects of experimental rainfall manipulations on Chihuahuan Desert grassland and shrubland plant communities |
| Q36308687 | Effects of increased flooding on riparian vegetation: Field experiments simulating climate change along five European lowland streams. |
| Q35784119 | Effects of nitrogen and phosphorus additions on soil microbial biomass and community structure in two reforested tropical forests |
| Q35215577 | Effects of nitrogen and phosphorus fertilization on soil carbon fractions in alpine meadows on the Qinghai-Tibetan Plateau |
| Q56776971 | Effects of nutrient loading and extreme rainfall events on coastal tallgrass prairies: invasion intensity, vegetation responses, and carbon and nitrogen distribution |
| Q33286158 | Effects of nutrients, herbivory, and depth on the macroalgal community in the rocky sublittoral |
| Q46411621 | Effects of resource addition on recovery of production and plant functional composition in degraded semiarid grasslands. |
| Q91912367 | Effects of soil nitrogen on diploid advantage in fireweed, Chamerion angustifolium (Onagraceae) |
| Q30959270 | Elevated CO2 reduces losses of plant diversity caused by nitrogen deposition |
| Q35868985 | Elevated carbon dioxide is predicted to promote coexistence among competing species in a trait-based model |
| Q34664159 | Energy potential of biomass from conservation grasslands in Minnesota, USA |
| Q33286427 | Environmental and plant community determinants of species loss following nitrogen enrichment |
| Q56974572 | Environmental costs and benefits of transportation biofuel production from food- and lignocellulose-based energy crops. A review |
| Q56437711 | Erosion of beta diversity under interacting global change impacts in a semi-arid grassland |
| Q56978123 | Evolutionary responses to land use in eight common grassland plants |
| Q33752311 | Experimental and observational studies find contrasting responses of soil nutrients to climate change |
| Q91773250 | Experimentally derived nitrogen critical loads for northern Great Plains vegetation |
| Q35010910 | Facilitation as a ubiquitous driver of biodiversity |
| Q46849215 | Fertilizer addition lessens the flux of microbial carbon to higher trophic levels in soil food webs of grassland |
| Q57262392 | Fewer new species colonize at low frequency N addition in a temperate grassland |
| Q57144537 | Foliar Nitrogen Responses to the Environmental Gradient Matrix of the Adirondack Park, New York |
| Q89660214 | Formation of Common Mycorrhizal Networks Significantly Affect Plant Biomass and Soil Properties of the Neighboring Plants under Various Nitrogen Levels |
| Q39042299 | Functional diversity increases ecological stability in a grazed grassland. |
| Q34513555 | Functional gene differences in soil microbial communities from conventional, low-input, and organic farmlands |
| Q46305132 | Functional traits determine tree growth and ecosystem productivity of a tropical montane forest: Insights from a long-term nutrient manipulation experiment. |
| Q51610231 | Fungal and bacterial growth responses to N fertilization and pH in the 150-year 'Park Grass' UK grassland experiment. |
| Q92709048 | Global change effects on plant communities are magnified by time and the number of global change factors imposed |
| Q30890163 | Global environmental change and the nature of aboveground net primary productivity responses: insights from long-term experiments |
| Q56460575 | Going beyond taxonomic diversity: deconstructing biodiversity patterns reveals the true cost of iceplant invasion |
| Q59282806 | Grass-legume mixtures impact soil N, species recruitment, and productivity in temperate steppe grassland |
| Q47826106 | Grassland establishment under varying resource availability: a test of positive and negative feedback. |
| Q57018573 | Grassland management intensification weakens the associations among the diversities of multiple plant and animal taxa |
| Q35815042 | Grazing maintains native plant diversity and promotes community stability in an annual grassland. |
| Q41607178 | Herbivores rescue diversity in warming tundra by modulating trait-dependent species losses and gains. |
| Q36061609 | Herbivory and nutrient limitation protect warming tundra from lowland species' invasion and diversity loss |
| Q33916395 | Hierarchical plant responses and diversity loss after nitrogen addition: testing three functionally-based hypotheses in the Inner Mongolia grassland |
| Q34432257 | How do sheep affect plant communities and arthropod populations in temperate grasslands? |
| Q37729927 | Immobilizing nitrogen to control plant invasion |
| Q35624774 | Impact of nitrogen deposition on forest and lake food webs in nitrogen-limited environments |
| Q57051824 | Impact of simulated changes in rainfall regime and nutrient deposition on the relative dominance and isotopic composition of ruderal plants in anthropogenic grasslands |
| Q36325546 | Impacts of 120 years of fertilizer addition on a temperate grassland ecosystem. |
| Q58380199 | Impacts of atmospheric nitrogen deposition: responses of multiple plant and soil parameters across contrasting ecosystems in long-term field experiments |
| Q31027283 | Impacts of weather on long-term patterns of plant richness and diversity vary with location and management |
| Q47328295 | Incorporating clonal growth form clarifies the role of plant height in response to nitrogen addition |
| Q33765801 | Increased primary production shifts the structure and composition of a terrestrial arthropod community |
| Q30378021 | Increased soil nutrition and decreased light intensity drive species loss after eight years grassland enclosures |
| Q57262406 | Increasing Soil Nutrient Loads of European Semi-natural Grasslands Strongly Alter Plant Functional Diversity Independently of Species Loss |
| Q35843368 | Influences of nitrogen, phosphorus and silicon addition on plant productivity and species richness in an alpine meadow |
| Q58264946 | Interactions between elevated atmospheric CO2 and defoliation on North American rangeland plant species at low and high N availability |
| Q56394993 | Interactions of arbuscular mycorrhizal fungi, critical loads of nitrogen deposition, and shifts from native to invasive species in a southern California shrubland |
| Q35648853 | Intransitive competition is widespread in plant communities and maintains their species richness |
| Q39596502 | Invaded grassland communities have altered stability-maintenance mechanisms but equal stability compared to native communities |
| Q57262190 | Invertebrate, not small vertebrate, herbivory interacts with nutrient availability to impact tallgrass prairie community composition and forb biomass |
| Q91583373 | Lasting signature of planting year weather on restored grasslands |
| Q44984618 | Leaf functional trait variation associated with salt tolerance in perennial ryegrass |
| Q26799303 | Life-history evolution in the anthropocene: effects of increasing nutrients on traits and trade-offs |
| Q46448559 | Light asymmetry explains the effect of nutrient enrichment on grassland diversity |
| Q30376599 | Linking the influence and dependence of people on biodiversity across scales. |
| Q30315220 | Locally rare species influence grassland ecosystem multifunctionality |
| Q56755085 | Long-Term Ecological Research in a Human-Dominated World |
| Q58573067 | Long-Term Nitrogen Fertilization Elevates the Activity and Abundance of Nitrifying and Denitrifying Microbial Communities in an Upland Soil: Implications for Nitrogen Loss From Intensive Agricultural Systems |
| Q57055703 | Long-term effects of species loss on community properties across contrasting ecosystems |
| Q30860101 | Long-term exposure to elevated CO2 enhances plant community stability by suppressing dominant plant species in a mixed-grass prairie |
| Q34450774 | Long-term nitrogen addition leads to loss of species richness due to litter accumulation and soil acidification in a temperate steppe |
| Q34808125 | Long-term nitrogen amendment alters the diversity and assemblage of soil bacterial communities in tallgrass prairie |
| Q33318652 | Loss of plant species after chronic low-level nitrogen deposition to prairie grasslands |
| Q57046572 | Management Intensity Modifies Plant Diversity Effects on N Yield and Mineral N in Soil |
| Q56763692 | Management intensity affects the relationship between non-native and native species in subtropical wetlands |
| Q46267290 | Maternal experience and soil origin influence interactions between resident species and a dominant invasive species |
| Q28709362 | Mechanisms for success after long-term nutrient enrichment in a boreal forest understory |
| Q30628812 | Microbial abundance and composition influence litter decomposition response to environmental change |
| Q56458665 | Microbial activity and soil respiration under nitrogen addition in Alaskan boreal forest |
| Q46809335 | Microbial responses to nitrogen addition in three contrasting grassland ecosystems. |
| Q64984058 | Mowing mitigates the negative impacts of N addition on plant species diversity. |
| Q56417991 | Native and alien herbaceous plants in the Brazilian Cerrado are (co-)limited by different nutrients |
| Q39302734 | Native plants fare better against an introduced competitor with native microbes and lower nitrogen availability |
| Q60523670 | Negative density dependence mediates biodiversity–productivity relationships across scales |
| Q38952566 | Nitrogen Critical Loads for an Alpine Meadow Ecosystem on the Tibetan Plateau |
| Q36721253 | Nitrogen addition and warming independently influence the belowground micro-food web in a temperate steppe |
| Q92605274 | Nitrogen addition decreases seed germination in a temperate steppe |
| Q45781990 | Nitrogen and phosphorus enrichment alter the composition of ammonia-oxidizing bacteria in salt marsh sediments. |
| Q34376709 | Nitrogen deposition alters plant-fungal relationships: linking belowground dynamics to aboveground vegetation change. |
| Q34628307 | Nitrogen deposition alters soil chemical properties and bacterial communities in the Inner Mongolia grassland. |
| Q46812967 | Nitrogen deposition potentially contributes to oak regeneration failure in the Midwestern temperate forests of the USA. |
| Q33739316 | Nitrogen deposition, competition and the decline of a regionally threatened legume, Desmodium cuspidatum |
| Q51119400 | Nitrogen enrichment modifies plant community structure via changes to plant-soil feedback. |
| Q58315402 | Nitrogen fertilization interacts with light to increase Rubus spp. cover in a temperate forest |
| Q28584605 | Nitrogen:phosphorous supply ratio and allometry in five alpine plant species |
| Q45061280 | Non-random species loss in a forest herbaceous layer following nitrogen addition |
| Q58798961 | Nutrient Dependent Cross-Kingdom Interactions: Fungi and Bacteria From an Oligotrophic Desert Oasis |
| Q31147055 | Nutrient limitation of native and invasive N2-fixing plants in northwest prairies |
| Q34405871 | Nutrient presses and pulses differentially impact plants, herbivores, detritivores and their natural enemies |
| Q92220483 | Nutrient-induced shifts of dominant species reduce ecosystem stability via increases in species synchrony and population variability |
| Q92795046 | Nutrients mitigate the impacts of extreme drought on plant invasions |
| Q56969394 | On the relationship between farmland biodiversity and land-use intensity in Europe |
| Q35597187 | Over 150 years of long-term fertilization alters spatial scaling of microbial biodiversity |
| Q57007963 | PLANT AND MICROBE CONTRIBUTION TO COMMUNITY RESILIENCE IN A DIRECTIONALLY CHANGING ENVIRONMENT |
| Q56701973 | Patterns of trait convergence and divergence among native and exotic species in herbaceous plant communities are not modified by nitrogen enrichment |
| Q43445973 | Perturbations alter community convergence, divergence, and formation of multiple community states |
| Q57019009 | Phragmites australis: How do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? |
| Q33300558 | Phylogenetic diversity of bacteria isolates from the Qinghai-Tibet Plateau permafrost region |
| Q30278830 | Plant Functional Diversity Can Be Independent of Species Diversity: Observations Based on the Impact of 4-Yrs of Nitrogen and Phosphorus Additions in an Alpine Meadow |
| Q30829573 | Plant Physiological, Morphological and Yield-Related Responses to Night Temperature Changes across Different Species and Plant Functional Types |
| Q36086201 | Plant community and soil chemistry responses to long-term nitrogen inputs drive changes in alpine bacterial communities |
| Q54288341 | Plant community responses to increased precipitation and belowground litter addition: Evidence from a 5-year semiarid grassland experiment. |
| Q34803960 | Plant community responses to long-term fertilization: changes in functional group abundance drive changes in species richness |
| Q35999143 | Plant diversity effects on grassland productivity are robust to both nutrient enrichment and drought |
| Q39359054 | Plant hydraulic responses to long-term dry season nitrogen deposition alter drought tolerance in a Mediterranean-type ecosystem |
| Q40350460 | Plant nitrogen concentration and isotopic composition in residential lawns across seven US cities |
| Q34595371 | Plant traits mediate consumer and nutrient control on plant community productivity and diversity |
| Q90179418 | Plant-microbe networks in soil are weakened by century-long use of inorganic fertilizers |
| Q31049710 | Plant-plant interactions and environmental change |
| Q91530087 | Potential vulnerability of 348 herbaceous species to atmospheric deposition of nitrogen and sulfur in the United States |
| Q51110253 | Prediction of extinction in plants: interaction of extrinsic threats and life history traits. |
| Q38950975 | Press-pulse interactions: effects of warming, N deposition, altered winter precipitation, and fire on desert grassland community structure and dynamics |
| Q46458575 | Productivity and species richness in longleaf pine woodlands: resource-disturbance influences across an edaphic gradient |
| Q50052693 | Random species loss underestimates dilution effects of host diversity on foliar fungal diseases under fertilization |
| Q33399225 | Rank clocks and plant community dynamics |
| Q35125689 | Realistic diversity loss and variation in soil depth independently affect community-level plant nitrogen use. |
| Q57051481 | Recasting the dynamic equilibrium model through a functional lens: the interplay of trait-based community assembly and climate |
| Q33814625 | Recovery of plant diversity following N cessation: effects of recruitment, litter, and elevated N cycling |
| Q34003660 | Recovery of plant species richness during long-term fertilization of a species-rich grassland |
| Q46772258 | Reduced compensatory effects explain the nitrogen-mediated reduction in stability of an alpine meadow on the Tibetan Plateau |
| Q34247275 | Relationship between reproductive allocation and relative abundance among 32 species of a Tibetan alpine meadow: effects of fertilization and grazing |
| Q39115559 | Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe |
| Q91874891 | Replacements of small- by large-ranged species scale up to diversity loss in Europe's temperate forest biome |
| Q118110125 | Reproductive height determines the loss of clonal grasses with nitrogen enrichment in a temperate grassland |
| Q45188287 | Resource availability and imbalance affect plant-mycorrhizal interactions: a field test of three hypotheses |
| Q31001704 | Resource colimitation governs plant community responses to altered precipitation |
| Q57411464 | Resource competition and community response to fertilization: the outcome depends on spatial strategies |
| Q56779725 | Response of the herbaceous layer of forest ecosystems to excess nitrogen deposition |
| Q48056954 | Response to nitrogen addition reveals metabolic and ecological strategies of soil bacteria. |
| Q56331377 | Responses of common and rare aliens and natives to nutrient availability and fluctuations |
| Q91225360 | Responses of diversity, productivity, and stability to the nitrogen input in a tropical grassland |
| Q57238096 | Responses of soil microbial community to nitrogen fertilizer and precipitation regimes in a semi-arid steppe |
| Q63389740 | Reversal of nitrogen-induced species diversity declines mediated by change in dominant grass and litter |
| Q35942276 | Rhizosphere bacterial communities of dominant steppe plants shift in response to a gradient of simulated nitrogen deposition. |
| Q33232116 | Richness and species composition of arboreal arthropods affected by nutrients and predators: a press experiment |
| Q43598978 | Risk-based determination of critical nitrogen deposition loads for fire spread in southern California deserts |
| Q50645935 | Role of AMT1;1 in NH4+ acquisition in Arabidopsis thaliana. |
| Q33362949 | Scale-dependent responses of plant biodiversity to nitrogen enrichment |
| Q34981838 | Sensitivity of grassland plant community composition to spatial vs. temporal variation in precipitation |
| Q30825233 | Shifts in grassland invasibility: effects of soil resources, disturbance, composition, and invader size |
| Q90291486 | Short-term, low-level nitrogen deposition dampens a trophic cascade between bears and plants |
| Q64118569 | Small mammal herbivores mediate the effects of soil nitrogen and invertebrate herbivores on grassland diversity |
| Q56447051 | Soil fertility alters the nature of plant–resource interactions in invaded grassland communities |
| Q90517501 | Soil heterogeneity increases plant diversity after 20 years of manipulation during grassland restoration |
| Q46812964 | Spatial gradient in nitrogen deposition affects plant species frequency in acidic grasslands. |
| Q51028876 | Species decline under nitrogen fertilization increases community-level competence of fungal diseases. |
| Q57068300 | Stability of tallgrass prairie during a 19-year increase in growing season precipitation |
| Q43696772 | Stochastic and deterministic processes together determine alpine meadow plant community composition on the Tibetan Plateau |
| Q44094092 | Teasing apart plant community responses to N enrichment: the roles of resource limitation, competition and soil microbes |
| Q34436428 | Testing mechanisms of N-enrichment-induced species loss in a semiarid Inner Mongolia grassland: critical thresholds and implications for long-term ecosystem responses |
| Q34473900 | Testing the paradox of enrichment along a land use gradient in a multitrophic aboveground and belowground community. |
| Q46429576 | The consequence of species loss on ecosystem nitrogen cycling depends on community compensation |
| Q28818015 | The contribution of nitrogen deposition to the eutrophication signal in understorey plant communities of European forests |
| Q116672606 | The effect of precipitation timing on phylogenetic and functional community structure in a semi-arid steppe |
| Q35135363 | The effects of insects, nutrients, and plant invasion on community structure and function above-and belowground |
| Q56437758 | The effects of species properties and community context on establishment success |
| Q51582672 | The impact of agricultural intensification and land-use change on the European arable flora. |
| Q36319890 | The role of above-ground competition and nitrogen vs. phosphorus enrichment in seedling survival of common European plant species of semi-natural grasslands |
| Q56742214 | The roles of exotic grasses and forbs when restoring native species to highly invaded southern California annual grassland |
| Q30276064 | Tight coupling of leaf area index to canopy nitrogen and phosphorus across heterogeneous tallgrass prairie communities |
| Q35023753 | Topography- and management-mediated resource gradients maintain rare and common plant diversity around paddy terraces |
| Q35553177 | Trait-based analysis of decline in plant species ranges during the 20th century: a regional comparison between the UK and Estonia |
| Q34890074 | Trait-based tests of coexistence mechanisms. |
| Q58315409 | Twenty-five-year response of the herbaceous layer of a temperate hardwood forest to elevated nitrogen deposition |
| Q58313615 | Using lichen functional diversity to assess the effects of atmospheric ammonia in Mediterranean woodlands |
| Q36196490 | Warming and fertilization alter the dilution effect of host diversity on disease severity. |
| Q28315408 | Woody encroachment decreases diversity across North American grasslands and savannas |
| Q58645392 | “Brown” World Invertebrates Contradict “Green” World Biodiversity Theory |