| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1003173110 |
| P356 | DOI | 10.1038/35071062 |
| P698 | PubMed publication ID | 11298447 |
| P5875 | ResearchGate publication ID | 12036633 |
| P50 | author | David Tilman | Q1176859 |
| Shibu Jose | Q110811614 | ||
| David A. Wedin | Q114441029 | ||
| Jean Knops | Q117284753 | ||
| Dan Bahauddin | Q117284754 | ||
| George Hendrey | Q117284755 | ||
| Keith Wrage | Q117284756 | ||
| Jenny Goth | Q117284757 | ||
| Wendy Bengston | Q117284758 | ||
| Joseph M. Craine | Q42850388 | ||
| Mark G. Tjoelker | Q47117729 | ||
| Shahid Naeem | Q47708028 | ||
| Peter B. Reich | Q51690278 | ||
| David S. Ellsworth | Q56756251 | ||
| Tali D Lee | Q57205782 | ||
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| P433 | issue | 6830 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | ecosystem | Q37813 |
| biodiversity | Q47041 | ||
| plant diversity | Q99658977 | ||
| ecosystem response | Q124100324 | ||
| P6104 | maintained by WikiProject | WikiProject Ecology | Q10818384 |
| P1104 | number of pages | 2 | |
| P304 | page(s) | 809-810 | |
| P577 | publication date | 2001-04-12 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Plant diversity enhances ecosystem responses to elevated CO2 and nitrogen deposition | |
| P478 | volume | 410 |
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| Q47460562 | Aboveground–belowground interactions as a source of complementarity effects in biodiversity experiments |
| Q92568372 | Abrupt declines in marine phytoplankton production driven by warming and biodiversity loss in a microcosm experiment |
| Q28597774 | Adaptation to elevated CO2 in different biodiversity contexts |
| Q33187426 | Additive effects of simulated climate changes, elevated CO2, and nitrogen deposition on grassland diversity |
| Q35045008 | Advancing biodiversity-ecosystem functioning science using high-density tree-based experiments over functional diversity gradients |
| Q28770114 | Ammonia-oxidizing bacteria respond to multifactorial global change |
| Q31002887 | BUGS in the analysis of biodiversity experiments: species richness and composition are of similar importance for grassland productivity |
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| Q31064125 | Biodiversity impacts ecosystem productivity as much as resources, disturbance, or herbivory |
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| Q56965499 | Biodiversity, Nitrogen Deposition, and CO2 Affect Grassland Soil Carbon Cycling but not Storage |
| Q28770157 | Biography of David Tilman |
| Q57196599 | Biological soil crusts (biocrusts) as a model system in community, landscape and ecosystem ecology |
| Q57196689 | Biomass responses to elevated CO2, soil heterogeneity and diversity: an experimental assessment with grassland assemblages |
| Q37510796 | Biotic vs. abiotic control of decomposition: a comparison of the effects of simulated extinctions and changes in temperature |
| Q51652270 | CO2, nitrogen, and diversity differentially affect seed production of prairie plants. |
| Q39558003 | Can complementarity in water use help to explain diversity-productivity relationships in experimental grassland plots? |
| Q34016572 | Changes in plant species richness induce functional shifts in soil nematode communities in experimental grassland |
| Q58648806 | Changes in soil microbial substrate utilization in response to altered litter diversity and precipitation in a Mediterranean shrubland |
| Q30912428 | Characterization of an urban-rural CO2/temperature gradient and associated changes in initial plant productivity during secondary succession |
| Q36915414 | Colloquium paper: resistance, resilience, and redundancy in microbial communities |
| Q31112653 | Compensatory responses to loss of warming-sensitive plant species |
| Q46274203 | Competitive network determines the direction of the diversity-function relationship |
| Q35942255 | Complementarity among four highly productive grassland species depends on resource availability |
| Q57179267 | Complementarity in both plant and mycorrhizal fungal communities are not necessarily increased by diversity in the other |
| Q110027451 | Complex climatic and CO2 controls on net primary productivity of temperate dryland ecosystems over central Asia during 1980–2014 |
| Q34366786 | Complex facilitation and competition in a temperate grassland: loss of plant diversity and elevated CO2 have divergent and opposite effects on oak establishment |
| Q56965894 | Conventional functional classification schemes underestimate the relationship with ecosystem functioning |
| Q56965256 | Daily environmental conditions determine the competition-facilitation balance for plant water status |
| Q56942843 | Decoupling the direct and indirect effects of nitrogen deposition on ecosystem function |
| Q56502723 | Development and applications of functional gene microarrays in the analysis of the functional diversity, composition, and structure of microbial communities |
| Q36369286 | Disentangling species and functional group richness effects on soil N cycling in a grassland ecosystem. |
| Q28658818 | Distinct responses of soil microbial communities to elevated CO2 and O3 in a soybean agro-ecosystem |
| Q55128112 | Divergent Responses of the Diazotrophic Microbiome to Elevated CO2 in Two Rice Cultivars. |
| Q57262257 | Diverse marsh plant communities are more consistently productive across a range of different environmental conditions through functional complementarity |
| Q33425994 | Diversity effects in early- and mid-successional species pools along a nitrogen gradient |
| Q56911682 | Diversity-biomass relationship across forest layers: implications for niche complementarity and selection effects |
| Q56483770 | EFFECTS OF GRASSLAND PLANT SPECIES DIVERSITY, ABUNDANCE, AND COMPOSITION ON FOLIAR FUNGAL DISEASE |
| Q30959210 | Ecology. Biodiversity under global change |
| Q34255771 | Ecology. Impacts of biodiversity loss |
| Q49167404 | Ecology. Price put on biodiversity |
| Q57111715 | Effects of Elevated Atmospheric CO2 on Microbial Community Structure at the Plant-Soil Interface of Young Beech Trees (Fagus sylvatica L.) Grown at Two Sites with Contrasting Climatic Conditions |
| Q56966093 | Effects of elevated CO2, nitrogen deposition, and decreased species diversity on foliar fungal plant disease |
| Q31048078 | Effects of elevated atmospheric carbon dioxide on biomass and carbon accumulation in a model regenerating longleaf pine community. |
| Q55368521 | Effects of increased temperature on plant communities depend on landscape location and precipitation. |
| Q34625049 | Effects of plant diversity, N fertilization, and elevated carbon dioxide on grassland soil N cycling in a long-term experiment |
| Q35621652 | Effects of plant diversity, functional group composition, and fertilization on soil microbial properties in experimental grassland |
| Q56965908 | Effects of plant species diversity, atmospheric [CO2], and N addition on gross rates of inorganic N release from soil organic matter |
| Q33277856 | Effects of species richness and elevated carbon dioxide on biomass accumulation: a synthesis using meta-analysis |
| Q56966099 | Elevated CO2 and plant species richness impact arbuscular mycorrhizal fungal spore communities |
| Q58264970 | Elevated CO2 effects on semi-arid grassland plants in relation to water availability and competition |
| Q30959270 | Elevated CO2 reduces losses of plant diversity caused by nitrogen deposition |
| Q56965579 | Elevated CO2 stimulates grassland soil respiration by increasing carbon inputs rather than by enhancing soil moisture |
| Q28681509 | Elevated CO₂ influences microbial carbon and nitrogen cycling |
| Q56965916 | Elevated [CO2] and increased N supply reduce leaf disease and related photosynthetic impacts on Solidago rigida |
| Q56965822 | Elevated atmospheric CO2: a nurse plant substitute for oak seedlings establishing in old fields |
| Q51331866 | Elevated carbon dioxide accelerates the spatial turnover of soil microbial communities. |
| Q34151269 | Elevated carbon dioxide alters the structure of soil microbial communities |
| Q39972989 | Elevated carbon dioxide concentrations indirectly affect plant fitness by altering plant tolerance to herbivory. |
| Q35868985 | Elevated carbon dioxide is predicted to promote coexistence among competing species in a trait-based model |
| Q52381770 | Elevated tropospheric CO2 and O3 concentrations impair organic pollutant removal from grassland soil. |
| Q31149722 | Empirical evaluation of a new method for calculating signal-to-noise ratio for microarray data analysis |
| Q58407982 | Evaluating ecosystem responses to rising atmospheric CO2 and global warming in a multi-factor world |
| Q58185525 | Evaluating the Benefits of Organic Farming in Rice Agroecosystems in the Philippines |
| Q33381177 | Evolutionary history and the effect of biodiversity on plant productivity |
| Q35209294 | Exotic plants contribute positively to biodiversity functions but reduce native seed production and arthropod richness |
| Q57019942 | Experimental evidence rejects pairwise modelling approach to coexistence in plant communities |
| Q31143076 | Experimental fire increases soil carbon dioxide efflux in a grassland long-term multifactor global change experiment |
| Q46849215 | Fertilizer addition lessens the flux of microbial carbon to higher trophic levels in soil food webs of grassland |
| Q35544691 | Flooding disturbances increase resource availability and productivity but reduce stability in diverse plant communities |
| Q46403816 | Food webs obscure the strength of plant diversity effects on primary productivity |
| Q58317529 | Food-chain length alters community responses to global change in aquatic systems |
| Q56942031 | Fragmentation modulates the strong impact of habitat quality and plant cover on fertility and microbial activity of semiarid gypsum soils |
| Q34014811 | Functional and phylogenetic diversity as predictors of biodiversity--ecosystem-function relationships |
| Q89493527 | Functional groups differ in trait means, but not in trait plasticity to species richness in local grassland communities |
| Q35987812 | Functional identity is the main driver of diversity effects in young tree communities |
| Q33716971 | Functional molecular ecological networks |
| Q58109559 | Functional responses of plants to elevated atmospheric CO2- do photosynthetic and productivity data from FACE experiments support early predictions? |
| Q35172168 | Fungal communities respond to long-term CO2 elevation by community reassembly |
| Q46340614 | Fungal interactions reduce carbon use efficiency |
| Q33567621 | GeoChip 3.0 as a high-throughput tool for analyzing microbial community composition, structure and functional activity |
| Q35093016 | GeoChip 4: a functional gene-array-based high-throughput environmental technology for microbial community analysis |
| Q35289962 | Global biodiversity, stoichiometry and ecosystem function responses to human-induced C-N-P imbalances. |
| Q47460589 | Global change belowground: impacts of elevated CO2, nitrogen, and summer drought on soil food webs and biodiversity |
| Q31115931 | Global-change drivers of ecosystem functioning modulated by natural variability and saturating responses |
| Q56966249 | Grassland species effects on soil CO2 flux track the effects of elevated CO2 and nitrogen |
| Q50788533 | Herbivore control of annual grassland composition in current and future environments. |
| Q31029454 | High plant diversity is needed to maintain ecosystem services |
| Q33329759 | Higher effect of plant species diversity on productivity in natural than artificial ecosystems |
| Q47460591 | Impact of above- and below-ground invertebrates on temporal and spatial stability of grassland of different diversity |
| Q58060504 | Impact of doubled CO2on global-scale leaf area index and evapotranspiration: Conflicting stomatal conductance and LAI responses |
| Q34255780 | Impacts of biodiversity loss escalate through time as redundancy fades |
| Q39400865 | Improved water retention links high species richness with increased productivity in arctic tundra moss communities. |
| Q30983088 | Increased rainfall variability and N addition accelerate litter decomposition in a restored prairie |
| Q60562107 | Increasing CO2 from subambient to superambient concentrations alters species composition and increases above-ground biomass in a C3/C4 grassland |
| Q33772664 | Increasing native, but not exotic, biodiversity increases aboveground productivity in ungrazed and intensely grazed grasslands |
| Q46985926 | Indirect effects drive evolutionary responses to global change |
| Q57027155 | Interactive effects of diversity, nutrients and elevated CO2 on experimental plant communities |
| Q30989668 | Interactive effects of elevated CO2 and precipitation change on leaf nitrogen of dominant Stipa L. species |
| Q33317024 | Interactive effects of plant species diversity and elevated CO2 on soil biota and nutrient cycling. |
| Q35848550 | Interspecific competition in phytoplankton drives the availability of essential mineral and biochemical nutrients |
| Q30913577 | Intraspecific litter diversity and nitrogen deposition affect nutrient dynamics and soil respiration. |
| Q56966114 | Legume presence increases photosynthesis and N concentrations of co-occurring non-fixers but does not modulate their responsiveness to carbon dioxide enrichment |
| Q90325905 | Limited evidence for spatial resource partitioning across temperate grassland biodiversity experiments |
| Q41481200 | Linking primary producer diversity and food quality effects on herbivores: A biochemical perspective |
| Q30376599 | Linking the influence and dependence of people on biodiversity across scales. |
| Q46837543 | Living close to your neighbors: the importance of both competition and facilitation in plant communities |
| Q57055703 | Long-term effects of species loss on community properties across contrasting ecosystems |
| Q40217805 | Long-term nitrogen deposition linked to reduced water use efficiency in forests with low phosphorus availability |
| Q39866225 | Macroclimate associated with urbanization increases the rate of secondary succession from fallow soil. |
| Q57046572 | Management Intensity Modifies Plant Diversity Effects on N Yield and Mineral N in Soil |
| Q45970696 | Mapping Functional Similarity of Predators on the Basis of Trait Similarities |
| Q28751782 | Marine biodiversity-ecosystem functions under uncertain environmental futures |
| Q35734156 | Mechanisms driving diversity-productivity relationships differ between exotic and native communities and are affected by gastropod herbivory |
| Q56966056 | Mechanisms responsible for the positive diversity-productivity relationship in Minnesota grasslands |
| Q30628812 | Microbial abundance and composition influence litter decomposition response to environmental change |
| Q30984683 | Microbial composition alters the response of litter decomposition to environmental change. |
| Q33262650 | Mycorrhizal fungal identity and richness determine the diversity and productivity of a tallgrass prairie system |
| Q56964230 | N deposition and elevated CO2on methane emissions: Differential responses of indirect effects compared to direct effects through litter chemistry feedbacks |
| Q56966059 | Nitrogen deposition and plant species interact to influence soil carbon stabilization |
| Q40334408 | Nitrogen limitation constrains sustainability of ecosystem response to CO2. |
| Q57036597 | Nitrogen uptake by grassland communities: contribution of N2 fixation, facilitation, complementarity, and species dominance |
| Q57027036 | Non-random species extinction and plant production: implications for ecosystem functioning |
| Q34789120 | Nutrient enrichment, biodiversity loss, and consequent declines in ecosystem productivity |
| Q56783734 | Opposite relationships between invasibility and native species richness at patch versus landscape scales |
| Q58105755 | Options and Constraints for Crop Diversification: A Case Study in Sustainable Agriculture in Uzbekistan |
| Q57027044 | Overyielding in experimental grassland communities - irrespective of species pool or spatial scale |
| Q34276872 | Parasite diversity and coinfection determine pathogen infection success and host fitness. |
| Q36106254 | Per capita interactions and stress tolerance drive stress-induced changes in biodiversity effects on ecosystem functions. |
| Q56966067 | Photosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated pCO2 across four free-air CO2 enrichment experiments in forest, grassland and desert |
| Q28742134 | Phylogenetic molecular ecological network of soil microbial communities in response to elevated CO2 |
| Q30619389 | Plant diversity does not buffer drought effects on early-stage litter mass loss rates and microbial properties |
| Q30977165 | Plant diversity drives soil microbial biomass carbon in grasslands irrespective of global environmental change factors |
| Q35999143 | Plant diversity effects on grassland productivity are robust to both nutrient enrichment and drought |
| Q28707839 | Plant diversity effects on soil food webs are stronger than those of elevated CO2 and N deposition in a long-term grassland experiment |
| Q30984676 | Plant diversity effects on soil microbial functions and enzymes are stronger than warming in a grassland experiment |
| Q60049453 | Plant diversity maintains multiple soil functions in future environments |
| Q27437875 | Plant diversity surpasses plant functional groups and plant productivity as driver of soil biota in the long term |
| Q33283700 | Plant diversity, CO2, and N influence inorganic and organic N leaching in grasslands |
| Q35604963 | Plant ecology. Anthropogenic environmental changes affect ecosystem stability via biodiversity |
| Q34000012 | Plant identity influences decomposition through more than one mechanism |
| Q39911093 | Plant responses to soil heterogeneity and global environmental change |
| Q47460588 | Plant species richness, elevated CO2, and atmospheric nitrogen deposition alter soil microbial community composition and function |
| Q56965854 | Plant species richness, elevated CO2, and atmospheric nitrogen deposition alter soil microbial community composition and function |
| Q30313839 | Plants are less negatively affected by flooding when growing in species-rich plant communities |
| Q50725709 | Predator biodiversity strengthens herbivore suppression. |
| Q51150399 | Quantifying effects of biodiversity on ecosystem functioning across times and places. |
| Q60348801 | Quantifying the effects of elevated CO2on water budgets by combining FACE data with an ecohydrological model |
| Q36332596 | Rainfall variability counteracts N addition by promoting invasive Lonicera maackii and extending phenology in prairie |
| Q57187540 | Reconciling plant strategy theories of Grime and Tilman |
| Q112594091 | Reduced CO2 fertilization effect in temperate C3 grasslands under more extreme weather conditions |
| Q57559747 | Reduced N cycling in response to elevated CO2, warming, and drought in a Danish heathland: Synthesizing results of the CLIMAITE project after two years of treatments |
| Q56462688 | Refuge for native lady beetles (Coccinellidae) in perennial grassland habitats |
| Q36061051 | Resource Availability Alters Biodiversity Effects in Experimental Grass-Forb Mixtures |
| Q55031851 | Resource Heterogeneity Moderates the Biodiversity-Function Relationship in Real World Ecosystems. |
| Q36102011 | Response of plant nutrient stoichiometry to fertilization varied with plant tissues in a tropical forest |
| Q56958982 | Responses of aboveground C and N pools to rainfall variability and nitrogen deposition are mediated by seasonal precipitation and plant community dynamics |
| Q24816863 | Responses of grassland production to single and multiple global environmental changes |
| Q33194182 | Scale-dependence of resource-biodiversity relationships |
| Q57447076 | Seasonal and inter-annual variability in litter decomposition and nitrogen availability in a mid-Appalachian watershed |
| Q35014106 | Separating direct and indirect effects of global change: a population dynamic modeling approach using readily available field data |
| Q33925988 | Seven years of carbon dioxide enrichment, nitrogen fertilization and plant diversity influence arbuscular mycorrhizal fungi in a grassland ecosystem |
| Q31000195 | Shifting grassland plant community structure drives positive interactive effects of warming and diversity on aboveground net primary productivity |
| Q56965943 | Soil Processes Affected by Sixteen Grassland Species Grown under Different Environmental Conditions |
| Q33913897 | Soil microbes drive the classic plant diversity-productivity pattern |
| Q91216109 | Soil microbial restoration strategies for promoting climate-ready prairie ecosystems |
| Q57196704 | Spatial heterogeneity in soil nutrient supply modulates nutrient and biomass responses to multiple global change drivers in model grassland communities |
| Q33204258 | Species and functional group diversity independently influence biomass accumulation and its response to CO2 and N. |
| Q26777169 | Species coexistence in a changing world |
| Q34284051 | Species composition and fire: non-additive mixture effects on ground fuel flammability |
| Q58391221 | Species of plants and associated arbuscular mycorrhizal fungi mediate mycorrhizal responses to CO2 enrichment |
| Q57027135 | Species vs community perspectives in biodiversity experiments |
| Q57026131 | Species-rich dung beetle communities buffer ecosystem services in perturbed agro-ecosystems |
| Q33263634 | Stoichiometric response of nitrogen-fixing and non-fixing dicots to manipulations of CO2, nitrogen, and diversity |
| Q58387346 | Temperate grasslands and global atmospheric change: a review |
| Q58247693 | Testing interactive effects of global environmental changes on soil nitrogen cycling |
| Q34541255 | Testing the link between functional diversity and ecosystem functioning in a Minnesota grassland experiment. |
| Q35747765 | The Diversity and Co-occurrence Patterns of N₂-Fixing Communities in a CO₂-Enriched Grassland Ecosystem |
| Q58686931 | The Effects of Plant-Soil-Enzyme Interactions on Plant Composition, Biomass and Diversity of Alpine Meadows in the Qinghai-Tibetan Plateau |
| Q35978741 | The diversity-disease relationship: evidence for and criticisms of the dilution effect. |
| Q36354730 | The economic value of grassland species for carbon storage. |
| Q91739999 | The fate of carbon in a mature forest under carbon dioxide enrichment |
| Q22064504 | The functional role of producer diversity in ecosystems |
| Q56965865 | The impact of elevated CO2, increased nitrogen availability and biodiversity on plant tissue quality and decomposition |
| Q34729886 | The need for comprehensive and consistent treatment of the nitrogen cycle in nitrogen cycling and mass balance studies: I. Terrestrial nitrogen cycle |
| Q56966284 | The response of soil CO2flux to changes in atmospheric CO2, nitrogen supply and plant diversity |
| Q35023753 | Topography- and management-mediated resource gradients maintain rare and common plant diversity around paddy terraces |
| Q47098193 | Toward a methodical framework for comprehensively assessing forest multifunctionality |
| Q51680714 | Transgenerational effects of global environmental change: long-term CO(2) and nitrogen treatments influence offspring growth response to elevated CO(2). |
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| Q74224131 | correction: Plant diversity enhances ecosystem responses to elevated CO2 and nitrogen deposition |
| Q28732745 | The phylogenetic composition and structure of soil microbial communities shifts in response to elevated carbon dioxide. |
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