| 1 | Native trees are responsible for the high carbon density in urban natural area forests across eight United States cities | 2.8 | 9 | Citations (PDF) |
| 2 | Antagonistic biotic interactions mitigate the positive effects of warming on wood decomposition | 1.3 | 0 | Citations (PDF) |
| 3 | Sustainable forest management for carbon, wood and biodiversity must consider natural disturbance regimes | 2.8 | 5 | Citations (PDF) |
| 4 | A diverse and distinct microbiome inside living trees | 30.6 | 33 | Citations (PDF) |
| 5 | Plant nitrogen demand, not soil carbon availability, decouples net mineralization and nitrification following forest canopy disturbances | 2.4 | 2 | Citations (PDF) |
| 6 | Zoogeochemical niche construction: how animal-mediated biogeochemistry affects evolution | 4.1 | 5 | Citations (PDF) |
| 7 | A stoichiometric approach to estimate sources of mineral‐associated soil organic matter | 7.4 | 76 | Citations (PDF) |
| 8 | Dominance of particulate organic carbon in top mineral soils in cold regions | 10.1 | 117 | Citations (PDF) |
| 9 | Plant functional type shapes nitrogen availability in a regenerating forest | 2.3 | 4 | Citations (PDF) |
| 10 | The importance of accounting method and sampling depth to estimate changes in soil carbon stocks | 3.3 | 32 | Citations (PDF) |
| 11 | A method for sampling the living wood microbiome | 3.3 | 10 | Citations (PDF) |
| 12 | Refining stoichiometric approaches to trace soil organic matter sources | 7.4 | 10 | Citations (PDF) |
| 13 | A common ericoid shrub modulates the diversity and structure of fungal communities across an arbuscular to ectomycorrhizal tree dominance gradient | 2.2 | 6 | Citations (PDF) |
| 14 | The biogeochemical boomerang: Site fidelity creates nutritional hotspots that may promote recurrent calving site reuse | 4.1 | 14 | Citations (PDF) |
| 15 | Local controls modify the effects of timber harvesting on surface soil carbon and nitrogen in a temperate hardwood forest | 2.6 | 4 | Citations (PDF) |
| 16 | Biogenic factors explain soil carbon in paired urban and natural ecosystems worldwide | 12.0 | 38 | Citations (PDF) |
| 17 | Quantifying the Effects Sizes of Common Controls on Methane Emissions From an Ombrotrophic Peat Bog | 2.0 | 7 | Citations (PDF) |
| 18 | Coarse woody debris accelerates the decomposition of deadwood inputs across temperate forest | 2.4 | 5 | Citations (PDF) |
| 19 | Depth‐dependent effects of ericoid mycorrhizal shrubs on soil carbon and nitrogen pools are accentuated under arbuscular mycorrhizal trees | 7.4 | 18 | Citations (PDF) |
| 20 | Mitigating near-term climate change | 2.8 | 5 | Citations (PDF) |
| 21 | Associations between recent land use history and urban forest composition | 5.2 | 13 | Citations (PDF) |
| 22 | Testing the feasibility of quantifying change in agricultural soil carbon stocks through empirical sampling | 5.0 | 43 | Citations (PDF) |
| 23 | Positive associations of soil organic matter and crop yields across a regional network of working farms | 1.8 | 48 | Citations (PDF) |
| 24 | Factors influencing the development and implementation of national greenhouse gas inventory methodologies | 1.1 | 5 | Citations (PDF) |
| 25 | Diverging conditions of current and potential future urban forest patches | 1.7 | 14 | Citations (PDF) |
| 26 | Myrmecochorous plants and their ant seed dispersers through successional stages in temperate cove forests | 1.0 | 3 | Citations (PDF) |
| 27 | The functional role of ericoid mycorrhizal plants and fungi on carbon and nitrogen dynamics in forests | 5.3 | 100 | Citations (PDF) |
| 28 | Patterns and controls of aboveground litter inputs to temperate forests | 2.4 | 16 | Citations (PDF) |
| 29 | Soil organic matter protects US maize yields and lowers crop insurance payouts under drought | 2.8 | 102 | Citations (PDF) |
| 30 | Signatures of an abiotic decomposition pathway in temperate forest leaf litter | 2.4 | 22 | Citations (PDF) |
| 31 | Quantifying microbial control of soil organic matter dynamics at macrosystem scales | 2.4 | 52 | Citations (PDF) |
| 32 | Positive long‐term impacts of restoration on soils in an experimental urban forest | 2.9 | 30 | Citations (PDF) |
| 33 | Ericoid mycorrhizal shrubs alter the relationship between tree mycorrhizal dominance and soil carbon and nitrogen | 3.0 | 36 | Citations (PDF) |
| 34 | Belowground community turnover accelerates the decomposition of standing dead wood | 2.4 | 27 | Citations (PDF) |
| 35 | Soil nutrient recovery after shelterwood timber harvesting in a temperate oak hardwood forest: Insights using a twenty-five-year chronosequence | 2.6 | 13 | Citations (PDF) |
| 36 | Natural Area Forests in US Cities: Opportunities and Challenges | 0.6 | 20 | Citations (PDF) |
| 37 | Estimating carbon storage in urban forests of New York City | 1.8 | 39 | Citations (PDF) |
| 38 | Scale dependence in functional equivalence and difference in the soil microbiome | 7.8 | 5 | Citations (PDF) |
| 39 | Improving scientific impact: How to practice science that influences environmental policy and management | 1.2 | 29 | Citations (PDF) |
| 40 | A trait-based understanding of wood decomposition by fungi | 5.2 | 191 | Citations (PDF) |
| 41 | Direct evidence using a controlled greenhouse study for threshold effects of soil organic matter on crop growth | 2.9 | 59 | Citations (PDF) |
| 42 | Disentangling resource acquisition from interspecific behavioral aggression to understand the ecological dominance of a common, widespread temperate forest ant | 0.8 | 10 | Citations (PDF) |
| 43 | Compensatory Thermal Adaptation of Soil Microbial Respiration Rates in Global Croplands | 4.1 | 32 | Citations (PDF) |
| 44 | Non-native Microstegium vimineum populations collapse with fungal leaf spot disease outbreak | 1.0 | 6 | Citations (PDF) |
| 45 | Field experiments show contradictory short‐ and long‐term myrmecochorous plant impacts on seed‐dispersing ants | 1.0 | 25 | Citations (PDF) |
| 46 | Evidence for the primacy of living root inputs, not root or shoot litter, in forming soil organic carbon | 5.3 | 553 | Citations (PDF) |
| 47 | Increasing microbial carbon use efficiency with warming predicts soil heterotrophic respiration globally | 7.4 | 81 | Citations (PDF) |
| 48 | Defining and assessing urban forests to inform management and policy | 2.8 | 47 | Citations (PDF) |
| 49 | The potential for mass ratio and trait divergence effects to explain idiosyncratic impacts of non‐native invasive plants on carbon mineralization of decomposing leaf litter | 2.9 | 18 | Citations (PDF) |
| 50 | Consistent trade-offs in fungal trait expression across broad spatial scales | 9.9 | 127 | Citations (PDF) |
| 51 | Arctic Soil Governs Whether Climate Change Drives Global Losses or Gains in Soil Carbon | 2.9 | 66 | Citations (PDF) |
| 52 | Global meta-analysis of the relationship between soil organic matter and crop yields | 2.7 | 641 | Citations (PDF) |
| 53 | Soil microbial respiration adapts to ambient temperature in global drylands | 7.6 | 129 | Citations (PDF) |
| 54 | Cross-biome patterns in soil microbial respiration predictable from evolutionary theory on thermal adaptation | 7.6 | 171 | Citations (PDF) |
| 55 | A city‐scale assessment reveals that native forest types and overstory species dominate New York City forests | 2.9 | 55 | Citations (PDF) |
| 56 | Nitrogen recycling in coupled green and brown food webs: Weak effects of herbivory and detritivory when nitrogen passes through soil | 3.0 | 16 | Citations (PDF) |
| 57 | Invasive lianas are drivers of and passengers to altered soil nutrient availability in urban forests | 1.3 | 22 | Citations (PDF) |
| 58 | Species associations overwhelm abiotic conditions to dictate the structure and function of wood‐decay fungal communities | 2.4 | 55 | Citations (PDF) |
| 59 | Long‐term research in ecology and evolution: a survey of challenges and opportunities | 6.9 | 87 | Citations (PDF) |
| 60 | Factors driving natural regeneration beneath a planted urban forest | 5.2 | 39 | Citations (PDF) |
| 61 | Acceleration or deceleration of litter decomposition by herbivory depends on nutrient availability through intraspecific differences in induced plant resistance traits | 3.0 | 23 | Citations (PDF) |
| 62 | Linking functional diversity and ecosystem processes: A framework for using functional diversity metrics to predict the ecosystem impact of functionally unique species | 3.0 | 60 | Citations (PDF) |
| 63 | Multiple models and experiments underscore large uncertainty in soil carbon dynamics | 2.4 | 238 | Citations (PDF) |
| 64 | Substrate identity and amount overwhelm temperature effects on soil carbon formation | 7.8 | 35 | Citations (PDF) |
| 65 | Understanding how microbiomes influence the systems they inhabit | 9.9 | 227 | Citations (PDF) |
| 66 | Microbial formation of stable soil carbon is more efficient from belowground than aboveground input | 10.1 | 789 | Citations (PDF) |
| 67 | Climate masks decomposer influence in a cross-site litter decomposition study | 7.8 | 72 | Citations (PDF) |
| 68 | Applying population and community ecology theory to advance understanding of belowground biogeochemistry | 4.1 | 86 | Citations (PDF) |
| 69 | Diversity begets diversity in competition for space | 7.6 | 101 | Citations (PDF) |
| 70 | Decoupling direct and indirect effects of temperature on decomposition | 7.8 | 38 | Citations (PDF) |
| 71 | Impacts of an invasive plant are fundamentally altered by a co‐occurring forest disturbance | 2.4 | 32 | Citations (PDF) |
| 72 | Competitive network determines the direction of the diversity–function relationship | 5.2 | 154 | Citations (PDF) |
| 73 | Long-Term Research in Ecology and Evolution (LTREE): 2015 survey data | 2.4 | 1 | Citations (PDF) |
| 74 | Nest-mediated seed dispersal | 1.0 | 9 | Citations (PDF) |
| 75 | Fungal interactions reduce carbon use efficiency | 4.1 | 117 | Citations (PDF) |
| 76 | Response of soil microbial community composition and function to a bottomland forest restoration intensity gradient | 3.7 | 90 | Citations (PDF) |
| 77 | A test of the hierarchical model of litter decomposition | 7.6 | 254 | Citations (PDF) |
| 78 | Identifying the microbial taxa that consistently respond to soil warming across time and space | 7.4 | 202 | Citations (PDF) |
| 79 | Direct effects of soil organic matter on productivity mirror those observed with organic amendments | 2.3 | 110 | Citations (PDF) |
| 80 | Quantifying global soil carbon losses in response to warming | 30.6 | 1,273 | Citations (PDF) |
| 81 | Understanding the dominant controls on litter decomposition | 3.0 | 585 | Citations (PDF) |
| 82 | A method for simultaneous measurement of soil bacterial abundances and community composition via 16S rRNA gene sequencing | 7.8 | 235 | Citations (PDF) |
| 83 | Greenhouse trace gases in deadwood | 2.4 | 44 | Citations (PDF) |
| 84 | Managing uncertainty in soil carbon feedbacks to climate change | 12.0 | 823 | Citations (PDF) |
| 85 | Opposing effects of different soil organic matter fractions on crop yields | 2.9 | 52 | Citations (PDF) |
| 86 | Practice patterns and complication rates of thrombolysis for pulmonary embolism | 1.1 | 6 | Citations (PDF) |
| 87 | Where, when and how plant–soil feedback matters in a changing world | 2.9 | 505 | Citations (PDF) |
| 88 | Cryptic indirect effects of exurban edges on a woodland community | 1.7 | 23 | Citations (PDF) |
| 89 | Growing the urban forest: tree performance in response to biotic and abiotic land management | 1.8 | 66 | Citations (PDF) |
| 90 | Compositional differences in simulated root exudates elicit a limited functional and compositional response in soil microbial communities | 2.9 | 36 | Citations (PDF) |
| 91 | Biotic interactions mediate soil microbial feedbacks to climate change | 5.2 | 254 | Citations (PDF) |
| 92 | Biofuel intercropping effects on soil carbon and microbial activity | 2.9 | 24 | Citations (PDF) |
| 93 | Farm management, not soil microbial diversity, controls nutrient loss from smallholder tropical agriculture | 2.9 | 27 | Citations (PDF) |
| 94 | Modelling the multidimensional niche by linking functional traits to competitive performance | 1.6 | 9 | Citations (PDF) |
| 95 | Environmental stress response limits microbial necromass contributions to soil organic carbon | 7.8 | 74 | Citations (PDF) |
| 96 | Climate history shapes contemporary leaf litter decomposition | 2.4 | 70 | Citations (PDF) |
| 97 | Agricultural intensification and the functional capacity of soil microbes on smallholder African farms | 2.8 | 54 | Citations (PDF) |
| 98 | Temperate forest termites: ecology, biogeography, and ecosystem impacts | 1.0 | 45 | Citations (PDF) |
| 99 | Consistent effects of eastern subterranean termites (Reticulitermes flavipes) on properties of a temperate forest soil | 7.8 | 18 | Citations (PDF) |
| 100 | Forest invader replaces predation but not dispersal services by a keystone species | 1.3 | 34 | Citations (PDF) |
| 101 | Reply to Veresoglou: Overdependence on “significance” testing in biology | 5.2 | 2 | Citations (PDF) |
| 102 | Mapping tree density at a global scale | 30.6 | 857 | Citations (PDF) |
| 103 | Microbial stoichiometry overrides biomass as a regulator of soil carbon and nitrogen cycling | 2.4 | 116 | Citations (PDF) |
| 104 | Disturbance Decouples Biogeochemical Cycles Across Forests of the Southeastern US | 1.7 | 46 | Citations (PDF) |
| 105 | Untangling the fungal niche: the trait-based approach | 2.9 | 252 | Citations (PDF) |
| 106 | Climate fails to predict wood decomposition at regional scales | 12.0 | 349 | Citations (PDF) |
| 107 | Competition as a mechanism structuring mutualisms | 3.0 | 34 | Citations (PDF) |
| 108 | Reply to Byrnes et al.: Aggregation can obscure understanding of ecosystem multifunctionality | 5.2 | 17 | Citations (PDF) |
| 109 | Do-Not-Resuscitate Status and Observational Comparative Effectiveness Research in Patients With Septic Shock* | 0.5 | 43 | Citations (PDF) |
| 110 | Positive effects of afforestation efforts on the health of urban soils | 2.6 | 63 | Citations (PDF) |
| 111 | Predicting the responsiveness of soil biodiversity to deforestation: a cross‐biome study | 7.4 | 125 | Citations (PDF) |
| 112 | Why are some microbes more ubiquitous than others? Predicting the habitat breadth of soil bacteria | 4.1 | 338 | Citations (PDF) |
| 113 | Mutualism fails when climate response differs between interacting species | 7.4 | 67 | Citations (PDF) |
| 114 | Biogeographic patterns in below-ground diversity in New York City's Central Park are similar to those observed globally | 1.6 | 347 | Citations (PDF) |
| 115 | Earthworms modify plant biomass and nitrogen capture under conditions of soil nutrient heterogeneity and elevated atmospheric CO 2 concentrations | 7.8 | 17 | Citations (PDF) |
| 116 | Discontinuity in the responses of ecosystem processes and multifunctionality to altered soil community composition | 5.2 | 219 | Citations (PDF) |
| 117 | Microbial communities may modify how litter quality affects potential decomposition rates as tree species migrate | 2.3 | 52 | Citations (PDF) |
| 118 | FORUM: Challenges and future directions in urban afforestation | 2.8 | 123 | Citations (PDF) |
| 119 | The effect of a quorum-quenching enzyme on leaf litter decomposition | 7.8 | 16 | Citations (PDF) |
| 120 | Empirical evidence that soil carbon formation from plant inputs is positively related to microbial growth | 2.4 | 265 | Citations (PDF) |
| 121 | Promoting Earth Stewardship through urban design experiments | 3.6 | 78 | Citations (PDF) |
| 122 | Science petitions are a facade of numbers | 30.6 | 3 | Citations (PDF) |
| 123 | Habitat, dispersal and propagule pressure control exotic plant infilling within an invaded range | 1.7 | 37 | Citations (PDF) |
| 124 | Thermal adaptation of decomposer communities in warming soils | 2.9 | 335 | Citations (PDF) |
| 125 | Thermal acclimation in widespread heterotrophic soil microbes | 4.1 | 215 | Citations (PDF) |
| 126 | Trophic cascade alters ecosystem carbon exchange | 5.2 | 106 | Citations (PDF) |
| 127 | Linking Predation Risk, Herbivore Physiological Stress and Microbial Decomposition of Plant Litter | 0.2 | 3 | Citations (PDF) |
| 128 | Animating the Carbon Cycle | 1.7 | 201 | Citations (PDF) |
| 129 | Social Insects Dominate Eastern US Temperate Hardwood Forest Macroinvertebrate Communities in Warmer Regions | 1.5 | 75 | Citations (PDF) |
| 130 | Linking Predation Risk, Herbivore Physiological Stress and Microbial Decomposition of Plant Litter | 0.2 | 1 | Citations (PDF) |
| 131 | Contingency in ecosystem but not plant community response to multiple global change factors | 5.3 | 19 | Citations (PDF) |
| 132 | Plant invasion impacts on arthropod abundance, diversity and feeding consistent across environmental and geographic gradients | 1.3 | 15 | Citations (PDF) |
| 133 | Grass Invasions Across a Regional Gradient are Associated with Declines in Belowground Carbon Pools | 1.7 | 30 | Citations (PDF) |
| 134 | Legacies of plant litter on carbon and nitrogen dynamics and the role of the soil community | 1.4 | 28 | Citations (PDF) |
| 135 | Elevated methane concentrations in trees of an upland forest | 2.9 | 130 | Citations (PDF) |
| 136 | Environmental Heterogeneity and Interspecific Interactions Influence Nest Occupancy By Key Seed-Dispersing Ants | 1.0 | 19 | Citations (PDF) |
| 137 | Root carbon flow from an invasive plant to belowground foodwebs | 2.3 | 40 | Citations (PDF) |
| 138 | Fear of Predation Slows Plant-Litter Decomposition | 26.1 | 245 | Citations (PDF) |
| 139 | The interaction between propagule pressure, habitat suitability and density‐dependent reproduction in species invasionOikos, 2012, 121, 874-881 | 1.6 | 73 | Citations (PDF) |
| 140 | The fate of glucose, a low molecular weight compound of root exudates, in the belowground foodweb of forests and pastures | 7.8 | 67 | Citations (PDF) |
| 141 | Decoupling litter barrier and soil moisture influences on the establishment of an invasive grass | 2.3 | 14 | Citations (PDF) |
| 142 | Performance and reproduction of an exotic invader across temperate forest gradients | 1.7 | 25 | Citations (PDF) |
| 143 | The effect of resource history on the functioning of soil microbial communities is maintained across time | 2.2 | 127 | Citations (PDF) |
| 144 | Universal Ecological Patterns in College Basketball Communities | 1.5 | 15 | Citations (PDF) |
| 145 | Differential Growth Responses of Soil Bacterial Taxa to Carbon Substrates of Varying Chemical Recalcitrance | 2.9 | 607 | Citations (PDF) |
| 146 | Temperature cues phenological synchrony in ant-mediated seed dispersal | 7.4 | 58 | Citations (PDF) |
| 147 | Temperature and soil organic matter decomposition rates - synthesis of current knowledge and a way forward | 7.4 | 1,453 | Citations (PDF) |
| 148 | Loss of faster-cycling soil carbon pools following grass invasion across multiple forest sites | 7.8 | 28 | Citations (PDF) |
| 149 | Soil fauna alter the effects of litter composition on nitrogen cycling in a mineral soil | 7.8 | 153 | Citations (PDF) |
| 150 | Nitrogen uptake and preference in a forest understory following invasion by an exotic grass | 1.3 | 56 | Citations (PDF) |
| 151 | The shape of things to come: woodland herb niche contraction begins during recruitment in mesic forest microhabitat | 1.6 | 39 | Citations (PDF) |
| 152 | Comparative metagenomic, phylogenetic and physiological analyses of soil microbial communities across nitrogen gradients | 5.9 | 1,807 | Citations (PDF) |
| 153 | Ant colonization and coarse woody debris decomposition in temperate forests | 0.8 | 48 | Citations (PDF) |
| 154 | Integrating microbial ecology into ecosystem models: challenges and priorities | 2.4 | 225 | Citations (PDF) |
| 155 | Rates of in situ carbon mineralization in relation to land-use, microbial community and edaphic characteristics | 7.8 | 53 | Citations (PDF) |
| 156 | Thermal adaptation of heterotrophic soil respiration in laboratory microcosms | 7.4 | 169 | Citations (PDF) |
| 157 | Grass invasion of a hardwood forest is associated with declines in belowground carbon pools | 7.4 | 89 | Citations (PDF) |
| 158 | Ant‐mediated seed dispersal does not facilitate niche expansion | 3.0 | 42 | Citations (PDF) |
| 159 | Soil-carbon response to warming dependent on microbial physiology | 10.1 | 1,484 | Citations (PDF) |
| 160 | Seasonal Climate Trends, the North Atlantic Oscillation, and Salamander Abundance in the Southern Appalachian Mountain Region | 0.4 | 18 | Citations (PDF) |
| 161 | The putative niche requirements and landscape dynamics of Microstegium vimineum: an invasive Asian grass | 1.3 | 63 | Citations (PDF) |
| 162 | Linkages between below and aboveground communities: Decomposer responses to simulated tree species loss are largely additive | 7.8 | 39 | Citations (PDF) |
| 163 | Surveying soil faunal communities using a direct molecular approach | 7.8 | 29 | Citations (PDF) |
| 164 | Empirical and theoretical challenges in aboveground–belowground ecology | 1.3 | 240 | Citations (PDF) |
| 165 | Litter quality is in the eye of the beholder: initial decomposition rates as a function of inoculum characteristics | 2.9 | 306 | Citations (PDF) |
| 166 | Decreased mass specific respiration under experimental warming is robust to the microbial biomass method employed | 4.1 | 19 | Citations (PDF) |
| 167 | Global patterns in belowground communities | 4.1 | 1,163 | Citations (PDF) |
| 168 | The influence of microbial communities, management, and soil texture on soil organic matter chemistry | 5.0 | 206 | Citations (PDF) |
| 169 | Testing the functional significance of microbial community composition | 2.4 | 709 | Citations (PDF) |
| 170 | Native, insect herbivore communities derive a significant proportion of their carbon from a widespread invader of forest understories | 1.3 | 21 | Citations (PDF) |
| 171 | Fungal Taxa Target Different Carbon Sources in Forest Soil | 1.7 | 193 | Citations (PDF) |
| 172 | Thermal adaptation of soil microbial respiration to elevated temperature | 4.1 | 792 | Citations (PDF) |
| 173 | Soil carbon stocks in experimental mesocosms are dependent on the rate of labile carbon, nitrogen and phosphorus inputs to soils | 2.9 | 273 | Citations (PDF) |
| 174 | Nonlinear root‐derived carbon sequestration across a gradient of nitrogen and phosphorous deposition in experimental mesocosms | 7.4 | 62 | Citations (PDF) |
| 175 | Global decomposition experiment shows soil animal impacts on decomposition are climate‐dependent | 7.4 | 466 | Citations (PDF) |
| 176 | Consequences of non‐random species loss for decomposition dynamics: experimental evidence for additive and non‐additive effects | 3.0 | 136 | Citations (PDF) |
| 177 | Direct and indirect effects of nitrogen deposition on litter decomposition | 7.8 | 115 | Citations (PDF) |
| 178 | Slow-cycle effects of foliar herbivory alter the nitrogen acquisition and population size of Collembola | 7.8 | 9 | Citations (PDF) |
| 179 | The influence of soil properties on the structure of bacterial and fungal communities across land-use types | 7.8 | 1,988 | Citations (PDF) |
| 180 | Nitrogen and Phosphorus Release from Mixed Litter Layers is Lower than Predicted from Single Species Decay | 1.7 | 45 | Citations (PDF) |
| 181 | Soil faunal assemblage composition modifies root in-growth to plant litter patches | 1.4 | 8 | Citations (PDF) |
| 182 | NONADDITIVE EFFECTS OF LEAF LITTER SPECIES DIVERSITY ON BREAKDOWN DYNAMICS IN A DETRITUS-BASED STREAM | 2.4 | 129 | Citations (PDF) |
| 183 | Carbon dynamics in a model grassland with functionally different soil communities | 2.9 | 35 | Citations (PDF) |
| 184 | TOWARD AN ECOLOGICAL CLASSIFICATION OF SOIL BACTERIA | 2.4 | 4,916 | Citations (PDF) |
| 185 | Impacts of invasive plant species on riparian plant assemblages: interactions with elevated atmospheric carbon dioxide and nitrogen deposition | 1.3 | 32 | Citations (PDF) |
| 186 | The abundance, richness and functional role of soil meso- and macrofauna in temperate grassland—A case study | 3.7 | 115 | Citations (PDF) |
| 187 | Decoupling the direct and indirect effects of nitrogen deposition on ecosystem function | 4.1 | 107 | Citations (PDF) |
| 188 | Soil heterogeneity and community composition jointly influence grassland biomass | 1.6 | 43 | Citations (PDF) |
| 189 | Soil nutrient heterogeneity interacts with elevated CO
2
and nutrient availability to determine species and assemblage responses in a model grassland community | 5.3 | 52 | Citations (PDF) |
| 190 | Do non-additive effects on decomposition in litter-mix experiments result from differences in resource quality between litters?Oikos, 2003, 102, 235-242 | 1.6 | 90 | Citations (PDF) |
| 191 | The adaptive response of a natural microbial population to carbon- and nitrogen-limitation | 4.1 | 41 | Citations (PDF) |
| 192 | Biodiversity and ecosystem productivity: implications for carbon storage | 1.6 | 128 | Citations (PDF) |
| 193 | Microbiota, fauna, and mesh size interactions in litter decomposition | 1.6 | 388 | Citations (PDF) |
| 194 | Assessing the functional implications of soil biodiversity in ecosystems | 1.0 | 26 | Citations (PDF) |
| 195 | Title is missing! | 2.3 | 149 | Citations (PDF) |
| 196 | The cross‐contamination and survival of
Salmonella enteritidis
PT4 on sterile and non‐sterile foodstuffs | 1.2 | 22 | Citations (PDF) |
| 197 | Soil organic carbon increases cereal yield stability regardless of tillage intensity | 5.4 | 1 | Citations (PDF) |
| 198 | Designing National Forest Inventories for Accurate Estimation of Soil Carbon Change | 7.4 | 0 | Citations (PDF) |
| 199 | Protecting wild populations and working landscapes: the case for transitioning to size-based criteria for federal regulation of American ginseng | 2.8 | 0 | Citations (PDF) |