| Aboveground impacts of a belowground invader: how invasive earthworms alter aboveground arthropod communities in a northern North American forest (DOI) |
| Predation increases multiple components of microbial diversity in activated sludge communities (DOI) |
| Biodiversity promotes ecosystem functioning despite environmental changes (DOI) |
| Effects of tree mixture on forest productivity: tree species addition versus substitution (DOI) |
| Climate adaptation of biodiversity conservation in managed forest landscapes (DOI) |
| The hidden role of multi-trophic interactions in driving diversity–productivity relationships (DOI) |
| Agriculture causes homogenization of plant-feedong nematode communities at regional scale (DOI) |
| Global daily 1 km land surface precipitation based on cloud cover-informed downscaling (DOI) |
| Tree planting in organic soils does not result in net carbon sequestration on decadal timescales (DOI) |
| Urgent need for updating the slogan of global climate actions from “tree planting” to “restore native vegetation” (DOI) |
| The role of urban trees in reducing land surface temperatures in European cities (DOI) |
| Maintaining forest cover to enhance temperature buffering under future climate change (DOI) |
| Multisubstrate DNA stable isotope probing reveals guild structure of bacteria that mediate soil carbon cycling (DOI) |
| Mycorrhizal symbiosis alleviates plant water deficit within and across generations via phenotypic plasticity (DOI) |
| Global patterns of resilience decline in vertebrate populations (DOI) |
| Niche difference determines coexistence and similar underlying processes in four ecological groups (DOI) |
| Diverse forests are cool: Promoting diverse forests to mitigate carbon emissions and climate change (DOI) |
| Deep learning-based quantification of arbuscular mycorrhizal fungi in plant roots (DOI) |
| CHELSA-W5E5 v1.0: W5E5 v1.0 downscaled with CHELSA v2.0 (DOI) |
| Microclimatic edge-to-interior gradients of European deciduous forests (DOI) |
| Low statistical power and overestimated anthropogenic impacts, exacerbated by publication bias, dominate field studies in global change biology (DOI) |
| Local stability properties of complex, species-rich soil food webs with functional block structure (DOI) |
| Functional diversity effects on productivity increase with age in a forest biodiversity experiment (DOI) |
| Biodiversity loss due to more than climate change (DOI) |
| Functional forest restoration (DOI) |
| Positive interactions are common among culturable bacteria (DOI) |
| Long-term, amplified responses of soil organic carbon to nitrogen addition worldwide (DOI) |
| Fractal triads efficiently sample ecological diversity and processes across spatial scales (DOI) |
| Microclimatic edge-to-interior gradients of European deciduous forests (DOI) |
| Local stability properties of complex, species-rich soil food webs with functional block structure (DOI) |
| Similarity of anthropogenic stressors is multifaceted and scale dependent (DOI) |
| Interaction network structure and spatial patterns influence invasiveness and invasibility in a stochastic model of plant communities (DOI) |
| Contributions and future priorities for soil science: Comparing perspectives from scientists and stakeholders (DOI) |
| Socioeconomic impacts of marine heatwaves: Global issues and opportunities (DOI) |
| Drought induces shifts in soil fungal communities that can be linked to root traits across 24 plant species (DOI) |
| Diversifying bioenergy crops increases yield and yield stability by reducing weed abundance (DOI) |
| Addressing context dependence in ecology (DOI) |
| Assessing the impact of grassland management on landscape multifunctionality (DOI) |
| Characterizing individual tree-level snags using airborne lidar-derived forest canopy gaps within closed-canopy conifer forests (DOI) |
| Nutrient enrichment increases invertebrate herbivory and pathogen damage in grasslands (DOI) |
| Do plant–soil interactions influence how the microbial community responds to environmental change? (DOI) |
| Biodiversity: Monitoring trends and implications for ecosystem functioning (DOI) |
| Plant herbivore protection by arbuscular mycorrhizas: a role for fungal diversity? (DOI) |
| Little effect of tree species richness on within- and between-plot variability in soil chemical properties in a young plantation forest (DOI) |
| Forest understorey communities respond strongly to light in interaction with forest structure, but not to microclimate warming (DOI) |
| Joint effects of climate, tree size, and year on annual tree growth derived from tree-ring records of ten globally distributed forests (DOI) |
| Arbuscular mycorrhizal tree communities have greater soil fungal diversity and relative abundances of saprotrophs and pathogens compared to ectomycorrhizal tree communities (DOI) |
| Microbial generalist or specialist: intraspecific variation and dormancy potential matter (DOI) |
| Contrasting effects of soil microbial interactions on growth–defence relationships between early- and mid-successional plant communities (DOI) |
| Handbook of field sampling for multi-taxon biodiversity studies in European forests (DOI) |
| The effect of periodic disturbances and carrying capacity on the significance of selection and drift in complex bacterial communities (DOI) |
| Substrate quality effects on stabilized soil carbon reverse with depth (DOI) |
| Mixing of tree species is especially beneficial for biodiversity in fragmented landscapes, without compromising forest functioning (DOI) |
| Little effect of tree species richness on within- and between-plot variability in soil chemical properties in a young plantation forest (DOI) |
| Root Carbon Interaction with Soil Minerals Is Dynamic, Leaving a Legacy of Microbially Derived Residues (DOI) |
| Temporal turnover of the soil microbiome composition is guild-specific (DOI) |
| ForestTemp – Sub-canopy microclimate temperatures of European forests (DOI) |
| Soil properties as key predictors of global grassland production: Have we overlooked micronutrients? (DOI) |
| Spatiotemporal origin of soil water taken up by vegetation (DOI) |
| Microbial storage and its implications for soil ecology (DOI) |
| The iDiv Ecotron—A flexible research platform for multitrophic biodiversity research (DOI) |
| Species identity and the functioning of ecosystems: the role of detritivore traits and trophic interactions in connecting of multiple ecosystem responses (DOI) |
| Persistence of plant-mediated microbial soil legacy effects in soil and inside roots (DOI) |
| Plant-microbe interactions in the phyllosphere: facing challenges of the anthropocene (DOI) |
| Combatting global grassland degradation (DOI) |
| The three major axes of terrestrial ecosystem function (DOI) |
| Microbial necromass as the source of soil organic carbon in global ecosystems (DOI) |
| Remotely detected plant function in two midwestern prairie grassland experiments reveals belowground processes (DOI) |
| Fading opportunities for mitigating agriculture-environment trade-offs in a south American deforestation hotspot (DOI) |
| Priority effects in microbiome assembly (DOI) |
| Phenotypic plasticity of fungal traits in response to moisture and temperature (DOI) |
| The soil microbiome — from metagenomics to metaphenomics (DOI) |
| Extinction of threatened vertebrates will lead to idiosyncratic changes in functional diversity across the world (DOI) |
| The importance of species interactions in eco-evolutionary community dynamics under climate change (DOI) |
| Links between microbial biomass and necromass components in the top- and subsoils of temperate grasslands along an aridity gradient (DOI) |
| Microbial tradeoffs in internal and external use of resources regulated by phosphorus and carbon availability (DOI) |
| Universal scaling of robustness of ecosystem services to species loss (DOI) |
| Tree species mixing affects soil microbial functioning indirectly via root and litter traits and soil parameters in European forests (DOI) |
| The Future of (Soil) Microbiome Studies: Current Limitations, Integration, and Perspectives (DOI) |
| Higher tree diversity increases soil microbial resistance to drought (DOI) |
| Comparing root exudate collection techniques: An improved hybrid method (DOI) |
| Include all fungi in biodiversity goals (DOI) |
| Large-scale drivers of relationships between soil microbial properties and organic carbon across Europe (DOI) |
| Plant developmental stage drives the differentiation in ecological role of the maize microbiome (DOI) |
| Belowground facilitation and trait matching: two or three to tango? (DOI) |
| Prolonged drought imparts lasting compositional changes to the rice root microbiome (DOI) |
| Spatial transcriptomics of planktonic and sessile bacterial populations at single-cell resolution (DOI) |
| Principles of seed banks and the emergence of complexity from dormancy (DOI) |
| An integrated framework of plant form and function: the belowground perspective (DOI) |
| Plant neighbours shape fungal assemblages associated with plant roots: A new understanding of niche-partitioning in plant communities (DOI) |
| Page 1 of 36 Representation of global change drivers across biodiversity datasets (DOI) |
| An integrated framework of plant form and function: the belowground perspective (DOI) |
| A unified framework for species spatial patterns: Linking the occupancy area curve, Taylor’s Law, the neighborhood density function and two-plot species turnover (DOI) |
| Plant pathogen infection risk tracks global crop yields under climate change (DOI) |
| Beyond organic farming – harnessing biodiversity-friendly landscapes (DOI) |
| Disturbance structures canopy and understory productivity along an environmental gradient (DOI) |
| Functional root trait-based classification of cover crops to improve soil physical properties (DOI) |
| Out of the dark: using energy flux to connect above‐ and belowground communities and ecosystem functioning (DOI) |
| Decomposition and transformations along the continuum from litter to soil organic matter in forest soils (DOI) |
| Unraveling negative biotic interactions determining soil microbial community assembly and functioning (DOI) |
| High consistency of trophic niches in soil microarthropod species (Oribatida, Acari) across soil depth and forest type (DOI) |
| Analysing continuous proportions in ecology and evolution: A practical introduction to beta and Dirichlet regression (DOI) |
| Grazing-induced biodiversity loss impairs grassland ecosystem stability at multiple scales (DOI) |
| Community composition influences ecosystem resistance and production more than species richness or intraspecific diversity (DOI) |
| Ecosystem coupling: A unifying framework to understand the functioning and recovery of ecosystems (DOI) |
| VNIR and MIR spectroscopy of PLFA-derived soil microbial properties and associated soil physicochemical characteristics in an experimental plant diversity gradient (DOI) |
| Drivers of seedling establishment success in dryland restoration efforts (DOI) |
| Spatial turnover of multiple ecosystem functions is more associated with plant than soil microbial β-diversity (DOI) |
| Microfluidic chips provide visual access to in situ soil ecology (DOI) |
| Above- and belowground biodiversity jointly tighten the P cycle in agricultural grasslands (DOI) |
| Nonlinear turnover rates of soil carbon following cultivation of native grasslands and subsequent afforestation of croplands (DOI) |
| Roots are key to increasing the mean residence time of organic carbon entering temperate agricultural soils (DOI) |
| Tree species richness promotes an early increase of stand structural complexity in young subtropical plantations (DOI) |
| Global homogenization of the structure and function in the soil microbiome of urban greenspaces (DOI) |
| Effects of Climate and Atmospheric Nitrogen Deposition on Early to Mid-Term Stage Litter Decomposition Across Biomes (DOI) |
| For the sake of resilience and multifunctionality, let’s diversify planted forests! (DOI) |
| How is litter decomposition affected by climate change in Mediterranean forests? Soil fauna has the key (DOI) |
| The impact of invertebrate decomposers on plants and soil (DOI) |
| Invasion theory as a management tool for increasing native biodiversity in urban ecosystems (DOI) |
| Coordination between compound-specific chemistry and morphology in plant roots aligns with ancestral mycorrhizal association in woody angiosperms (DOI) |
| Climate and land-use changes drive biodiversity turnover in arthropod assemblages over 150 years (DOI) |
| Contrasting effects of soil microbial interactions on growth-defence relationships between early- and mid-successional plant communities (DOI) |
| Natural soil microbiome variation affects spring foliar phenology with consequences for plant productivity and climate-driven range shifts (DOI) |
| Microclimate and land surface temperature in a biodiversity enriched oil palm plantation (DOI) |
| Seasonality affects specialisation of a temperate forest herbivore community (DOI) |
| Indirect effects of climate change inhibit N2 fixation associated with the feathermoss Hylocomium splendens in subarctic tundra (DOI) |
| Global homogenization of the structure and function in the soil microbiome of urban greenspaces (DOI) |
| Spatial extrapolation of topographic models for mapping soil organic carbon using local samples (DOI) |
| A microbiota–root–shoot circuit favours Arabidopsis growth over defence under suboptimal light (DOI) |
| Negative effects of nitrogen override positive effects of phosphorus on grassland legumes worldwide (DOI) |
| Soil burrow characterization by 3D image analysis: Prediction of macroinvertebrate groups from biopore size distribution parameters (DOI) |
| Ecology Letters. 2021;00:1–15. wileyonlinelibrary.com/journal/ele | 1 © 2021 John Wiley & Sons Ltd. INTRODUCTION Phenotypic plasticity, the ability of genotypes to express different phenotypes in response to the environment, is recognised as one of the key mechanisms by which plants can cope with the fast- changing climate (Hoffmann & Sgrò, 2011; Jump & Peñuelas, 2005) and other global change drivers (Matesanz et al., 2010). Knowledge of broad- scale drivers of phenotypic plasticity is therefore of utmost importance if we are to understand and predict plant responses to global change (Valladares et al., 2014). Although plants are generally plastic (Sultan, 2000), spe- cies and/or populations differ greatly in their levels of plasticity (Dostál et al., 2016; Gianoli & Valladares, 2012; Sultan, 2001; Valladares et al., 2000). These differences between species and/or populations may arise due to differences in selective pressures favouring the evolution of increased phenotypic plasticity, but also due to fac- tors limiting its evolution (Alpert & Simms, 2002; van Kleunen & Fischer, 2005; Valladares et al., 2007), which are rarely considered. The main factor known to select for the evolution of increased phenotypic plasticity is environmental het- erogeneity (Alpert & Simms, 2002; Vázquez et al., 2017). There is substantial evidence that climatic variability is positively associated with plant phenotypic plasticity (Alpert & Simms, 2002; Carvajal et al., 2017; Gianoli, 2004; Gianoli & González- Teuber, 2005; Lázaro- Nogal SYNTHESIS Global trends in phenotypic plasticity of plants (DOI) |
| Disentangling soil microbiome functions by perturbation (DOI) |
| Realities and hopes in the application of microbial tools in agriculture (DOI) |
| Direct and indirect effects of global change on mycorrhizal associations of savanna plant communities (DOI) |
| A hierarchical, multivariate meta-analysis approach to synthesizing global change experiments (DOI) |
| Coordination between compound-specific chemistry and morphology in plant roots aligns with ancestral mycorrhizal association in woody angiosperms (DOI) |
| Invertebrate decline reduces bacterial diversity associated with leaves and flowers (DOI) |
| A practical guide to question formation, systematic searching and study screening for literature reviews in ecology and evolution (DOI) |
| The flux of root-derived carbon via fungi and bacteria into soil microarthropods (Collembola) differs markedly between cropping systems (DOI) |
| Relative importance of tree species richness, tree functional type, and microenvironment for soil macrofauna communities in European forests (DOI) |
| Soil organic carbon response to global environmental change depends on its distribution between mineral-associated and particulate organic matter: A meta-analysis (DOI) |
| Contrasting responses of above- and belowground diversity to multiple components of land-use intensity (DOI) |
| Reconstruction of plant–pollinator networks from observational data (DOI) |
| Diversity increases yield but reduces harvest index in crop mixtures (DOI) |
| Conditioning the soil microbiome through plant–soil feedbacks suppresses an aboveground insect pest (DOI) |
| Rice rhizodeposition promotes the build-up of organic carbon in soil via fungal necromass (DOI) |
| Plant history and soil history jointly influence the selection environment for plant species in a long- term grassland biodiversity experiment (DOI) |
| Soil fauna diversity and chemical stressors: a review of knowledge gaps and roadmap for future research (DOI) |
| Biodiversity as insurance: from concept tomeasurement and application (DOI) |
| Biodiversity–productivity relationships are key to nature-based climate solutions (DOI) |
| Drought resistance and resilience: The role of soil moisture–plant interactions and legacies in a dryland ecosystem (DOI) |
| Three-dimensional soil heterogeneity modulates responses of grassland mesocosms to an experimentally imposed drought extreme (DOI) |
| Non-linear plant-plant interactions modulate impact of extreme drought and recovery on a Mediterranean ecosystem (DOI) |
| Targeted plant hologenome editing for plant trait enhancement (DOI) |
| Functional trait effects on ecosystem stability: assembling the jigsaw puzzle (DOI) |
| A novel trap design fornon‑lethal monitoring ofdung beetles using eDNA metabarcoding (DOI) |
| Variance, locality and structure: Three experimental challenges in the study of the response of soil microbial communities to multiple perturbations (DOI) |
| Do large herbivores maintain open habitats in temperate forests? (DOI) |
| The Democracy of Dirt: Relating Micro-Scale Dynamics to Macro-Scale Ecosystem Function (DOI) |
| Five years of whole-soil warming led to loss of subsoil carbon stocks and increased CO2 efflux (DOI) |
| The dimensionality and structure of species trait spaces (DOI) |
| Soil fauna modulates the effect of experimental drought on litter decomposition in forests invaded by an exotic pathogen (DOI) |
| Impact of land use type and organic farming on the abundance, diversity, community composition and functional properties of soil nematode communities in vegetable farming (DOI) |
| Global data on earthworm abundance, biomass, diversity and corresponding environmental properties (DOI) |
| Short-term intensive warming shifts predator communities (Parasitiformes: Mesostigmata) in boreal forest soils (DOI) |
| Soil texture affects the coupling of litter decomposition and soil organic matter formation (DOI) |
| Dynamic interactions at the mineral–organic matter interface (DOI) |
| Litter decomposition and infiltration capacities in soils of different tropical urban land covers (DOI) |
| Air-drying and long time preservation of soil do not significantly impact microbial community composition and structure (DOI) |
| Mixing tree species associated with arbuscular or ectotrophic mycorrhizae reveals dual mycorrhization and interactive effects on the fungal partners (DOI) |
| Changes inplant-herbivore network structure androbustness along land-use intensity gradients ingrasslands and forests (DOI) |
| Biodiversity and ecosystem functioning: Have our experiments and indices been underestimating the role of facilitation? (DOI) |
| Leaf trait variation in species-rich tropical Andean forests (DOI) |
| Genome wide association study reveals plant loci controlling heritability of the rhizosphere microbiome (DOI) |
| A holistic framework integrating plant-microbe-mineral regulation of soil bioavailable nitrogen (DOI) |
| A conceptual framework and experimental design for analysing the relationship between biodiversity and ecosystem functioning (BEF) in agroforestry systems (DOI) |
| Population dynamics of microbial cross-feeding are determined by co-localization probabilities and cooperation-independent cheater growth (DOI) |
| Metabolic flexibility allows bacterial habitat generalists to become dominant in a frequently disturbed ecosystem (DOI) |
| Linking functional traits and demography to model species-rich communities (DOI) |
| Increasing canopy mortality affects the future demographic structure of Europe’s forests (DOI) |
| The ecosystem services of urban soils: A review (DOI) |
| Separating the temperature response of soil respiration derived from soil organic matter and added labile carbon compounds (DOI) |
| Temperature Increases Soil Respiration Across Ecosystem Types and Soil Development, But Soil Properties Determine the Magnitude of This Effect (DOI) |
| Forest Carbon (DOI) |
| Restoring natural forests is the best way to remove atmospheric carbon (DOI) |
| Enabling sustainable agriculture through understanding and enhancement of microbiomes (DOI) |
| Intra-specific leaf trait responses to species richness at two different local scales (DOI) |
| Land-use drives the temporal stability and magnitude of soil microbial functions and modulates climate effects (DOI) |
| Relative importance of tree species richness, tree functional type, and microenvironment for soil macrofauna communities in European forests (DOI) |
| All together now: Limitations and recommendations for the simultaneous analysis of all eukaryotic soil sequences (DOI) |
| Incorporation of mineral nitrogen in soil food web as affected by plant community composition (DOI) |
| General statistical scaling laws for stability in ecological systems (DOI) |
| Microbe‐mediated adaptation in plants (DOI) |
| Responses of plant diversity to precipitation change are strongest at local spatial scales and in drylands (DOI) |
| How roots and shoots communicate through stressful times (DOI) |
| Universal rules of life: metabolic rates, biological times and the equal fitness paradigm (DOI) |
| Invertebrate functional traits and terrestrial nutrient cycling: Insights from a global meta‐analysis (DOI) |
| Bryophyte C:N:P stoichiometry, biogeochemical niches and elementome plasticity driven by environment and coexistence (DOI) |
| Latitudinal patterns of terrestrial phosphorus limitation over the globe (DOI) |
| Plant-Soil Feedbacks and Temporal Dynamics of Plant Diversity-Productivity Relationships (DOI) |
| Global groundwater wells at risk of running dry (DOI) |
| Projecting the continental accumulation of alien species through to 2050 (DOI) |
| Facilitation in the soil microbiome does not necessarily lead to niche expansion (DOI) |
| Changing elemental cycles, stoichiometric mismatches, and consequences for pathogens of primary producers (DOI) |
| Plant neighbors shape fungal assemblages associated with plant roots: a new understanding of niche‐partitioning in plant communities (DOI) |
| Overshooting tipping point thresholds in a changing climate (DOI) |
| Priming mechanisms providing plants and microbes access to mineral-associated organic matter (DOI) |
| Where Might We Find Ecologically Intact Communities? (DOI) |
| Effects of rising CO2 levels on carbon sequestration are coordinated above and below ground (DOI) |
| The megabiota are disproportionately important for biosphere functioning (DOI) |
| Physical protection of extracellular and intracellular DNA in soil aggregates against simulated natural oxidative processes (DOI) |
| Conserving intraspecific variation for nature’s contributions to people (DOI) |
| Metagenomic characterization of soil microbial communities in the Luquillo experimental forest (Puerto Rico) and implications for nitrogen cycling (DOI) |
| Soil microbial biomass and enzyme kinetics for the assessment of temporal diversification in agroecosystems (DOI) |
| Bark-dwelling methanotrophic bacteria decrease methane emissions from trees (DOI) |
| Soil moisture–atmosphere feedback dominates land carbon uptake variability (DOI) |
| Measurement and analysis of interspecific spatial associations as a facet of biodiversity (DOI) |
| Soil fauna diversity and chemical stressors: a review of knowledge gaps and roadmap for future research (DOI) |
| Diversity and identity of economics traits determine the extent of tree mixture effects on ecosystem productivity (DOI) |
| Diversity and asynchrony in soil microbial communities stabilizes ecosystem functioning (DOI) |
| Herbaceous perennial plants with short generation time have stronger responses to climate anomalies than those with longer generation time (DOI) |
| Better outcomes for pest pressure, insecticide use, and yield in less intensive agricultural landscapes (DOI) |
| Nutrient complexity triggers transitions between solitary and colonial growth in bacterial populations (DOI) |
| The significance of tree-tree interactions for forest ecosystem functioning (DOI) |
| Forest microclimates and climate change: Importance, drivers and future research agenda (DOI) |
| Experimental evidence of the importance of multitrophic structure for species persistence (DOI) |
| Cell size, genome size, and maximum growth rate are near‐independent dimensions of ecological variation across bacteria and archaea (DOI) |
| Erosion reduces soil microbial diversity, network complexity and multifunctionality (DOI) |
| Estimating maximal microbial growth rates from cultures, metagenomes, and single cells via codon usage patterns (DOI) |
| More diverse tree communities promote foliar fungal pathogen diversity, but decrease infestation rates per tree species, in a subtropical biodiversity experiment (DOI) |
| Biotic homogenization destabilizes ecosystem functioning by decreasing spatial asynchrony (DOI) |
| Beyond denitrification: The role of microbial diversity in controlling nitrous oxide reduction and soil nitrous oxide emissions (DOI) |
| Virtual pollination trade uncovers global dependence on biodiversity of developing countries (DOI) |
| Interactive Complex Heatmap package (DOI) |
| Biological mechanisms may contribute to soil carbon saturation patterns (DOI) |
| Scaling up biodiversity–ecosystem functioning relationships: the role of environmental heterogeneity in space and time (DOI) |
| Microbiota-root-shoot-environment axis and stress tolerance in plants (DOI) |
| Emerging strategies for precision microbiome management in diverse agroecosystems (DOI) |
| A multitaxa assessment of the effectiveness of agri-environmental schemes for biodiversity management (DOI) |
| Plant- or microbial-derived? A review on the molecular composition of stabilized soil organic matter (DOI) |
| Persistent organic pollutant cycling in forests (DOI) |
| Tree species richness modulates water supply in the local tree neighbourhood: evidence from wood δ13C signatures in a large-scale forest experiment (DOI) |
| Enhanced light interception and light use efficiency explain overyielding in young tree communities (DOI) |
| The Kroof experiment: realization and efficacy of a recurrentdrought experiment plus recovery in a beech/spruce forest (DOI) |
| Cumulative growth and stress responses to the 2018-2019 drought in a European floodplain forest (DOI) |
| Plant- or microbial-derived? A review on the molecular composition of stabilized soil organic matter (DOI) |
| Warming impairs trophic transfer efficiency in a long-term field experiment (DOI) |
| The Impact of Root-Derived Resources on Forest Soil Invertebrates Depends on Body Size and Trophic Position (DOI) |
| Enabling sustainable agriculture through understanding and enhancement of microbiomes (DOI) |
| Overyielding in young tree communities does not support the stress‐gradient hypothesis and is favoured by functional diversity and higher water availability (DOI) |
| Tree species richness modulates water supply in the local tree neighbourhood: evidence from wood δ13C signatures in a large-scale forest experiment (DOI) |
| Conserving intraspecific variation for nature’s contributions to people (DOI) |
| Soil-plant compartments affect fungal microbiome diversity and composition in grapevine (DOI) |
| The Ecology Underground coalition: building a collaborative future of belowground ecology and ecologists (DOI) |
| Evidence for a fungal loop in shrublands (DOI) |
| Earthworm invasion causes declines across soil fauna size classes and biodiversity facets in northern North American forests (DOI) |
| The reign of thep-value is over: what alternative analyses could we employ to fill the power vacuum? (DOI) |
| Pathways regulating decreased soil respiration with warming in a biocrust‐dominated dryland (DOI) |
| Soil organic carbon is not just for soil scientists: measurement recommendations for diverse practitioners (DOI) |
| Seed‐borne, endospheric and rhizospheric core microbiota as predictor for plant functional traits across rice cultivars are dominated by deterministic processes (DOI) |
| Community‐scale effects and strain: Facilitation beyond conspicuous patterns (DOI) |
| Local Tree Diversity Suppresses Foliar Fungal Infestation and Decreases Morphological But Not Molecular Richness in a Young Subtropical Forest (DOI) |
| Evolutionary priming and transition to the ectomycorrhizal habit in an iconic lineage of mushroom-forming fungi: is preadaptation a requirement? (DOI) |
| Root effects on soil organic carbon: a double‐edged sword (DOI) |
| Illuminating the intrinsic and extrinsic drivers of ecological stability across scales (DOI) |
| Consistent trait–environment relationships within and across tundra plant communities (DOI) |
| Feasibility of the 4 per 1000 aspirational target for soil carbon. A case study for France (DOI) |
| Microbial community response to a decade of simulated global changes depends on the plant community (DOI) |
| Climatic aridity increases temporal nestedness of invertebrate communities in naturally drying rivers (DOI) |
| Maximum CO2 diffusion inside leaves is limited by the scaling of cell size and genome size (DOI) |
| Search for top‐down and bottom‐up drivers of latitudinal trends in insect herbivory in oak trees in Europe (DOI) |
| A remote sensing derived data set of 100 million individual tree crowns for the National Ecological Observatory Network (DOI) |
| Plant, soil and faunal responses to a contrived pH gradient (DOI) |
| Priority effects and ecological restoration (DOI) |
| Facilitation and biodiversity–ecosystem function relationships in crop production systems and their role in sustainable farming (DOI) |
| The Temporal Dynamics of Multiple Stressor Effects: From Individuals to Ecosystems (DOI) |
| Identifying soil provenance based on portable X-ray fluorescence measurements using similarity and inverse-mapping approaches – A case in the Lower Hunter Valley, Australia (DOI) |
| Low forest productivity associated with increasing drought‐tolerant species is compensated by an increase in drought‐tolerance richness (DOI) |
| Global projections of the soil microbiome in the Anthropocene (DOI) |
| An interdisciplinary framework to describe and evaluate the functioning of forest ecosystems (DOI) |
| Balance between geographic, soil, and host tree parameters to shape soil microbiomes associated to clonal oak varies across soil zones along a European North‐South transect (DOI) |
| Aboveground litter inputs determine carbon storage across soil profiles: a meta-analysis (DOI) |
| Biodiversity facets affect community surface temperature via 3D canopy structure in grassland communities (DOI) |
| Plant evolution driven by interactions with symbiotic and pathogenic microbes (DOI) |
| Species identity, rather than species mixtures, drives cover crop effects on nutrient partitioning in unfertilized agricultural soil (DOI) |
| Root-released organic anions in response to low phosphorus availability: recent progress, challenges and future perspectives (DOI) |
| Shape of species climate response curves affects community response to climate change (DOI) |
| Niche differentiation of bacteria and fungi in carbon and nitrogen cycling of different habitats in a temperate coniferous forest: A metaproteomic approach (DOI) |
| C-offset and crop energy efficiency increase due industrial poultry waste use in long-term no-till soil minimizing environmental pollution (DOI) |
| The ‘soil health’ metaphor: illuminating or illusory? (DOI) |
| Application of residue, inorganic fertilizer and lime affect phosphorus solubilizing microorganisms and microbial biomass under different tillage and cropping systems in a Ferralsol (DOI) |
| Functional rarity and evenness are key facets of biodiversity to boost multifunctionality (DOI) |
| Soil microbial diversity–biomass relationships are driven by soil carbon content across global biomes (DOI) |
| Reprint of: Tree-tree interactions and crown complementarity: the role of functional diversity and branch traits for canopy packing (DOI) |
| Synergistic interactions between detritivores disappear under reduced rainfall (DOI) |
| The significance of tree-tree interactions for forest ecosystem functioning (DOI) |
| The Arctic Carbon Cycle and Its Response to Changing Climate (DOI) |
| Body size dependent dispersal influences stability in heterogeneous metacommunities (DOI) |
| C-STABILITY an innovative modeling framework to leverage the continuous representation of organic matter (DOI) |
| Nitrogen cycling microbiomes are structured by plant mycorrhizal associations with consequences for nitrogen oxide fluxes in forests (DOI) |
| Grazing and the vanishing complexity of plant association networks in grasslands (DOI) |
| Gross N transformations vary with soil moisture and time following urea deposition to a pasture soil (DOI) |
| Targeting the Active Rhizosphere Microbiome of Trifolium pratense in Grassland Evidences a Stronger-Than-Expected Belowground Biodiversity-Ecosystem Functioning Link (DOI) |
| Soil Texture, Sampling Depth and Root Hairs Shape the Structure of ACC Deaminase Bacterial Community Composition in Maize Rhizosphere (DOI) |
| Globally, plant‐soil feedbacks are weak predictors of plant abundance (DOI) |
| Soil chemical legacies trigger species‐specific and context‐dependent root responses in later arriving plants (DOI) |
| Temperature and pH define the realized niche space of arbuscular mycorrhizal fungi (DOI) |
| The forest and sustainable forestry (DOI) |
| Anthropogenic nitrogen enrichment increased the efficiency of belowground biomass production in a boreal forest (DOI) |
| Constraining human contributions to observed warming since the pre-industrial period (DOI) |
| Bumblebee colony density on farmland is influenced by late‐summer nectar supply and garden cover (DOI) |
| How much carbon input is required to preserve or increase projected soil organic carbon stocks in German croplands under climate change? (DOI) |
| Hydraulic diversity stabilizes productivity in a large-scale subtropical tree biodiversity experiment (DOI) |
| Root trait–microbial relationships across tundra plant species (DOI) |
| Tracking, targeting, and conserving soil biodiversity (DOI) |
| Biodiversity enhances the multitrophic control of arthropod herbivory. (DOI) |
| Complementary Roles of Wood-Inhabiting Fungi and Bacteria Facilitate Deadwood Decomposition (DOI) |
| Urban warming causes increased demand for lipids among dehydrated invertebrates (DOI) |
| Exploiting the full potential of Bayesian networks in predictive ecology (DOI) |
| Root traits explain rhizosphere fungal community composition among temperate grassland plant species (DOI) |
| Soil element coupling is driven by ecological context and atomic mass (DOI) |
| Organic Matter Degradation across Ecosystem Boundaries: The Need for a Unified Conceptualization (DOI) |
| Insect decline in the Anthropocene: Death by a thousand cuts (DOI) |
| News Feature: To understand the plight of insects, entomologists look to the past (DOI) |
| Agricultural intensification and climate change are rapidly decreasing insect biodiversity (DOI) |
| To us insectometers, it is clear that insect decline in our Costa Rican tropics is real, so let’s be kind to the survivors (DOI) |
| Insects and recent climate change (DOI) |
| The decline of butterflies in Europe: Problems, significance, and possible solutions (DOI) |
| A window to the world of global insect declines: Moth biodiversity trends are complex and heterogeneous (DOI) |
| Deep learning and computer vision will transform entomology (DOI) |
| No buzz for bees: Media coverage of pollinator decline (DOI) |
| Arthropods are not declining but are responsive to disturbance in the Luquillo Experimental Forest, Puerto Rico (DOI) |
| Insect biomass decline scaled to species diversity: General patterns derived from a hoverfly community (DOI) |
| Nonlinear trends in abundance and diversity and complex responses to climate change in Arctic arthropods (DOI) |
| Opinion: Eight simple actions that individuals can take to save insects from global declines (DOI) |
| Global distribution of earthworm diversity (DOI) |
| Topography and forest diversity facets regulate overstory and understory aboveground biomass in a temperate forest of South Korea (DOI) |
| Spatial and evolutionary predictability of phytochemical diversity (DOI) |
| Soil Microbes Generate Stronger Fitness Differencesthan Stabilization among California Annual Plants (DOI) |
| Unifying ecosystem responses to disturbance into a single statistical framework (DOI) |
| Different responses of soil carbon chemistry to fertilization regimes in the paddy soil and upland soil were mainly reflected by the opposite shifts of OCH and alkyl C (DOI) |
| Predator presence and recent climatic warming raise body temperatures of island lizards (DOI) |
| Divergent mineralization of hydrophilic and hydrophobic organic substrates and their priming effect in soils depending on their preferential utilization by bacteria and fungi (DOI) |
| Fungal Communities Are Important Determinants of Bacterial Community Composition in Deadwood (DOI) |
| Changes in soil fungal community composition depend on functional group and forest disturbance type (DOI) |
| Why Hypothesis Testers Should Spend Less Time Testing Hypotheses (DOI) |
| Organism body size structures the soil microbial and nematode community assembly at a continental and global scale (DOI) |
| Plant intraspecific competition and growth stage alter carbon and nitrogen mineralization in the rhizosphere (DOI) |
| How microbes can, and cannot, be used to assess soil health (DOI) |
| Light availability and light demand of plants shape the arbuscular mycorrhizal fungal communities in their roots (DOI) |
| Facts to acidification–induced carbonate losses from Chinese croplands (DOI) |
| Unifying ecosystem responses to disturbance into a single statistical framework (DOI) |
| Model representation and quantitative analysis of pore three‐dimensional morphological structure based on soil computed tomography images (DOI) |
| Forest fire induces short‐term shifts in soil food webs with consequences for carbon cycling (DOI) |
| Crop asynchrony stabilizes food production (DOI) |
| State of knowledge of soil biodiversity - Status, challenges and potentialities (DOI) |
| Biogeochemical cycling of phosphorus in subsoils of temperate forest ecosystems (DOI) |
| Substrate spatial heterogeneity reduces soil microbial activity (DOI) |
| How do Biotic and Abiotic FactorsRegulate Soil Enzyme Activitiesat Plot and Microplot Scales Under Afforestation? (DOI) |
| Global human-made mass exceeds all living biomass (DOI) |
| Above-belowground linkages of functionally dissimilar plant communities and soil properties in a grassland experiment (DOI) |
| A comparison between water uptake and root length density in winter wheat: effects of root density and rhizosphere properties (DOI) |
| How Introduced Earthworms Alter Ecosystems (DOI) |
| Fungal communities associated with roots of two closely related Juglandaceae species with a disjunct distribution in the tropics (DOI) |
| Quantifying organic carbon stocks using a stereological profile imaging method to account for rock fragments in stony soils (DOI) |
| Iron and aluminum association with microbially processed organic matter via meso-density aggregate formation across soils: organo-metallic glue hypothesis (DOI) |
| How competitive intransitivity and niche overlap affect spatial coexistence (DOI) |
| Alpha-, beta-, and gamma-diversity of bacteria varies across habitats (DOI) |
| Alarming evidence of widespread mite extinctions in the shadows of plant, insect and vertebrate extinctions (DOI) |
| Explainable artificial intelligence enhances the ecological interpretability of black‐box species distribution models (DOI) |
| Research Article Increased growing-season productivity drives earlier autumn leaf senescence in temperate trees (DOI) |
| Synergistic effects of four climate change drivers on terrestrial carbon cycling (DOI) |
| Grazed temporary grass‐clover leys in crop rotations can have a positive impact on soil quality under both conventional and organic agricultural systems (DOI) |
| Diversity and asynchrony in soil microbial communities stabilizes ecosystem functioning (DOI) |
| Springtails—Worldwide Jumpers (DOI) |
| Shining new light into soil systems: Spectroscopy in microfluidic soil chips reveals microbial biogeochemistry (DOI) |
| Host neighborhood shapes bacterial community assembly and specialization on tree species across a latitudinal gradient (DOI) |
| Assessing microbial residues in soil as a potential carbon sink and moderator of carbon use efficiency (DOI) |
| Species richness promotes ecosystem carbon storage: evidence from biodiversity-ecosystem functioning experiments (DOI) |
| Nitrogen addition alters composition, diversity, and functioning of microbial communities in mangrove soils: An incubation experiment (DOI) |
| Bypass and hyperbole in soil science: A perspective from the next generation of soil scientists (DOI) |
| From pools to flow: The PROMISE framework for new insights on soil carbon cycling in a changing world (DOI) |
| Climate warming negates arbuscular mycorrhizal fungal reductions in soil phosphorus leaching with tall fescue but not lucerne (DOI) |
| The characteristic time of ecological communities (DOI) |
| Strong priming of soil organic matter induced by frequent input of labile carbon (DOI) |
| Belowground competition favors character convergence but not character displacement in root traits (DOI) |
| The response of soil multi-functionality to agricultural management practices can be predicted by key soil abiotic and biotic properties (DOI) |
| Ten simple rules for increased lab resilience (DOI) |
| Effect of tree mixtures and water availability on belowground complementarity of fine roots of birch and pine planted on sandy podzol (DOI) |
| Nematodes as Drivers of Plant Performance in Natural Systems (DOI) |
| Drivers of carbon stocks in forest edges across Europe (DOI) |
| Impact of management of cover crop‐soybean agroecosystems on rhizosphere microbial communities (DOI) |
| Detritivore conversion of litter into faeces accelerates organic matter turnover (DOI) |
| Bacteria in Soil Keep Your Hamburger “Healthy” (DOI) |
| Methods and approaches to advance soil macroecology (DOI) |
| The multidimensionality of soil macroecology (DOI) |
| Soil aggregate-mediated microbial responses to long-term warming (DOI) |
