| Q28603185 | (A)synchronous Availabilities of N and P Regulate the Activity and Structure of the Microbial Decomposer Community |
| Q58756353 | A considerable fraction of soil-respired CO is not emitted directly to the atmosphere |
| Q55497160 | A moisture function of soil heterotrophic respiration that incorporates microscale processes. |
| Q57250251 | A plant–microbe interaction framework explaining nutrient effects on primary production |
| Q57498716 | A synoptic survey of microbial respiration, organic matter decomposition, and carbon efflux in U.S. streams and rivers |
| Q35150202 | Adjustment of microbial nitrogen use efficiency to carbon:nitrogen imbalances regulates soil nitrogen cycling |
| Q57579012 | Agronomic fortification of rice grains with secondary and micronutrients under differing crop management and soil moisture regimes in the north Indian Plains |
| Q30720658 | Altered precipitation regime affects the function and composition of soil microbial communities on multiple time scales |
| Q46801051 | Annual burning of a tallgrass prairie inhibits C and N cycling in soil, increasing recalcitrant pyrogenic organic matter storage while reducing N availability |
| Q30990358 | Application of a two-pool model to soil carbon dynamics under elevated CO2. |
| Q36376331 | Are variations in heterotrophic soil respiration related to changes in substrate availability and microbial biomass carbon in the subtropical forests? |
| Q92883151 | Bacterial metabolic state more accurately predicts antibiotic lethality than growth rate |
| Q49254723 | CO2 fixation in above-ground biomass of summer maize under different tillage and straw management treatments |
| Q39844297 | Carbon Availability Modifies Temperature Responses of Heterotrophic Microbial Respiration, Carbon Uptake Affinity, and Stable Carbon Isotope Discrimination. |
| Q92822135 | Carbon Use Efficiency and Its Temperature Sensitivity Covary in Soil Bacteria |
| Q36500683 | Carbon and nitrogen additions induce distinct priming effects along an organic-matter decay continuum |
| Q92238595 | Carbon control on terrestrial ecosystem function across contrasting site productivities: the carbon connection revisited |
| Q44251298 | Carbon use efficiency and storage in terrestrial ecosystems |
| Q34694221 | Carbon use efficiency of microbial communities: stoichiometry, methodology and modelling. |
| Q57201181 | Causes of variation in mineral soil C content and turnover in differently managed beech dominated forests |
| Q39492610 | Comparative Toxicities of Salts on Microbial Processes in Soil |
| Q36339298 | Contrasting effects of nitrogen addition on soil respiration in two Mediterranean ecosystems |
| Q58319894 | Decay rates of leaf litters from arbuscular mycorrhizal trees are more sensitive to soil effects than litters from ectomycorrhizal trees |
| Q90288696 | Defining trait-based microbial strategies with consequences for soil carbon cycling under climate change |
| Q36405580 | Differential sensitivity of total and active soil microbial communities to drought and forest management |
| Q37504387 | Disentangling the influence of earthworms in sugarcane rhizosphere. |
| Q28821222 | Distinct respiratory responses of soils to complex organic substrate are governed predominantly by soil architecture and its microbial community |
| Q58699414 | Divergent accumulation of microbial necromass and plant lignin components in grassland soils |
| Q35716675 | Do microorganism stoichiometric alterations affect carbon sequestration in paddy soil subjected to phosphorus input? |
| Q51292303 | Dual, differential isotope labeling shows the preferential movement of labile plant constituents into mineral-bonded soil organic matter. |
| Q57178408 | Dynamic, Intermediate Soil Carbon Pools May Drive Future Responsiveness to Environmental Change |
| Q58262749 | Ecoenzymatic stoichiometry and microbial processing of organic matter in northern bogs and fens reveals a common P-limitation between peatland types |
| Q53689243 | Effect of in-situ aged and fresh biochar on soil hydraulic conditions and microbial C use under drought conditions. |
| Q56937868 | Effects of litter traits, soil biota, and soil chemistry on soil carbon stocks at a common garden with 14 tree species |
| Q46254118 | Elevated moisture stimulates carbon loss from mineral soils by releasing protected organic matter |
| Q58264828 | Enhanced decomposition and nitrogen mineralization sustain rapid growth ofEucalyptus regnansafter wildfire |
| Q90447304 | Environmental effects on soil microbial nitrogen use efficiency are controlled by allocation of organic nitrogen to microbial growth and regulate gross N mineralization |
| Q28828937 | Enzymatic Strategies and Carbon Use Efficiency of a Litter-Decomposing Fungus Grown on Maize Leaves, Stems, and Roots |
| Q35730857 | Excess of Organic Carbon in Mountain Spruce Forest Soils after Bark Beetle Outbreak Altered Microbial N Transformations and Mitigated N-Saturation. |
| Q35752824 | Exotic grasses and nitrate enrichment alter soil carbon cycling along an urban-rural tropical forest gradient |
| Q28604252 | Experimental warming of a mountain tundra increases soil CO2 effluxes and enhances CH4 and N2O uptake at Changbai Mountain, China |
| Q28584233 | Field-Based Estimates of Global Warming Potential in Bioenergy Systems of Hawaii: Crop Choice and Deficit Irrigation |
| Q33603550 | Flexible Carbon-Use Efficiency across Litter Types and during Decomposition Partly Compensates Nutrient Imbalances-Results from Analytical Stoichiometric Models |
| Q56754915 | Following the Turnover of Soil Bioavailable Phosphate in Mediterranean Savanna by Oxygen Stable Isotopes |
| Q58403647 | Global soil carbon projections are improved by modelling microbial processes |
| Q64078198 | Global variation of soil microbial carbon-use efficiency in relation to growth temperature and substrate supply |
| Q90014171 | Glucose triggers strong taxon-specific responses in microbial growth and activity: insights from DNA and RNA qSIP |
| Q35787519 | Grass invasion effects on forest soil carbon depend on landscape-level land use patterns |
| Q46314404 | Growth and death of bacteria and fungi underlie rainfall-induced carbon dioxide pulses from seasonally dried soil |
| Q63849726 | Growth explains microbial carbon use efficiency across soils differing in land use and geology |
| Q36385498 | Historical climate controls soil respiration responses to current soil moisture. |
| Q35889485 | Historical precipitation predictably alters the shape and magnitude of microbial functional response to soil moisture |
| Q35922849 | Impact of long-term cropping of glyphosate-resistant transgenic soybean [Glycine max (L.) Merr.] on soil microbiome |
| Q90050533 | Implication of Viral Infections for Greenhouse Gas Dynamics in Freshwater Wetlands: Challenges and Perspectives |
| Q28818803 | Improvement in the biochemical and chemical properties of badland soils by thorny bamboo |
| Q56964056 | Incorporating microbial ecology concepts into global soil mineralization models to improve predictions of carbon and nitrogen fluxes |
| Q98169857 | Increase in abundance and decrease in richness of soil microbes following Hurricane Otto in three primary forest types in the Northern Zone of Costa Rica |
| Q92174770 | Increased microbial growth, biomass, and turnover drive soil organic carbon accumulation at higher plant diversity |
| Q58803732 | Increasing soil carbon storage: mechanisms, effects of agricultural practices and proxies. A review |
| Q46726695 | Integrating plant litter quality, soil organic matter stabilization, and the carbon saturation concept |
| Q30870042 | Interactions between temperature and nutrients across levels of ecological organization |
| Q51168109 | Introduction to a Virtual Special Issue on ecological stoichiometry and global change. |
| Q30652972 | Labile compounds in plant litter reduce the sensitivity of decomposition to warming and altered precipitation |
| Q58765423 | Land use driven change in soil pH affects microbial carbon cycling processes |
| Q35163363 | Linking annual N2O emission in organic soils to mineral nitrogen input as estimated by heterotrophic respiration and soil C/N ratio |
| Q28652177 | Living roots magnify the response of soil organic carbon decomposition to temperature in temperate grassland |
| Q58653091 | Local-scale determinants of elemental stoichiometry of soil in an old-growth temperate forest |
| Q33687371 | Michaelis-Menten kinetics of soil respiration feedbacks to nitrogen deposition and climate change in subtropical forests |
| Q34730076 | Microbial carbon mineralization in tropical lowland and montane forest soils of Peru |
| Q91999842 | Microbial carbon source utilization in rice rhizosphere and nonrhizosphere soils with short-term manure N input rate in paddy field |
| Q92509246 | Microbial carbon use efficiency predicted from genome-scale metabolic models |
| Q34678609 | Microbial community composition explains soil respiration responses to changing carbon inputs along an Andes-to-Amazon elevation gradient |
| Q35045009 | Microbial community dynamics alleviate stoichiometric constraints during litter decay |
| Q28657447 | Microbial community stratification linked to utilization of carbohydrates and phosphorus limitation in a boreal peatland at Marcell Experimental Forest, Minnesota, USA |
| Q35999944 | Microbial community structures and metabolic profiles response differently to physiochemical properties between three landfill cover soils |
| Q97681173 | Microbial diversity drives carbon use efficiency in a model soil |
| Q30835991 | Microbial dormancy improves development and experimental validation of ecosystem model |
| Q64921646 | Microbial ecoenzyme stoichiometry, nutrient limitation, and organic matter decomposition in wetlands of the conterminous United States. |
| Q35145339 | Microbial growth and carbon use efficiency in the rhizosphere and root-free soil |
| Q100694503 | Microbial growth and carbon use efficiency show seasonal responses in a multifactorial climate change experiment |
| Q41886976 | Microbial physiology and soil CO2 efflux after 9 years of soil warming in a temperate forest - no indications for thermal adaptations |
| Q31137312 | Microbial respiration, but not biomass, responded linearly to increasing light fraction organic matter input: Consequences for carbon sequestration |
| Q41693314 | Microbial technology with major potentials for the urgent environmental needs of the next decades |
| Q57059877 | Microbial temperature sensitivity and biomass change explain soil carbon loss with warming |
| Q51145672 | Model formulation of microbial CO2 production and efficiency can significantly influence short and long term soil C projections. |
| Q30868883 | Modeling adaptation of carbon use efficiency in microbial communities |
| Q40428724 | Multivariate regulation of soil CO2 and N2 O pulse emissions from agricultural soils. |
| Q59129092 | Nitrogen availability regulates topsoil carbon dynamics after permafrost thaw by altering microbial metabolic efficiency |
| Q28659584 | Nitrogen deposition enhances carbon sequestration by plantations in northern China |
| Q37054431 | Nitrogen deposition may enhance soil carbon storage via change of soil respiration dynamic during a spring freeze-thaw cycle period |
| Q56990806 | Nutrient availability as the key regulator of global forest carbon balance |
| Q46328755 | Optimal metabolic regulation along resource stoichiometry gradients. |
| Q26766195 | Organic nitrogen storage in mineral soil: Implications for policy and management |
| Q57014505 | Physiological shifts in the microbial community drive changes in enzyme activity in a perennial agroecosystem |
| Q30977165 | Plant diversity drives soil microbial biomass carbon in grasslands irrespective of global environmental change factors |
| Q35596157 | Plant diversity increases soil microbial activity and soil carbon storage |
| Q57066002 | Plant rhizosphere influence on microbial C metabolism: the role of elevated CO2, N availability and root stoichiometry |
| Q34994142 | Plant soil interactions alter carbon cycling in an upland grassland soil. |
| Q38944694 | Plant, microbial and ecosystem carbon use efficiencies interact to stabilize microbial growth as a fraction of gross primary production |
| Q46381085 | Plant-microbial competition for nitrogen increases microbial activities and carbon loss in invaded soils |
| Q39462040 | Rate of warming affects temperature sensitivity of anaerobic peat decomposition and greenhouse gas production. |
| Q46243346 | Resource Legacies of Organic and Conventional Management Differentiate Soil Microbial Carbon Use. |
| Q46451201 | Resource stoichiometry and the biogeochemical consequences of nitrogen deposition in a mixed deciduous forest |
| Q58572831 | Responses of Nitrogen-Cycling Microorganisms to Dazomet Fumigation |
| Q41380027 | Responses of belowground carbon allocation dynamics to extended shading in mountain grassland |
| Q59282788 | Responses of nitrous oxide emissions from crop rotation systems to four projected future climate change scenarios on a black Vertosol in subtropical Australia |
| Q57250258 | Short-term carbon input increases microbial nitrogen demand, but not microbial nitrogen mining, in a set of boreal forest soils |
| Q57435531 | Short-term nitrogen mineralization from warm-season cover crops in organic farming systems |
| Q34447597 | Short-term parasite-infection alters already the biomass, activity and functional diversity of soil microbial communities |
| Q27317173 | Social dynamics within decomposer communities lead to nitrogen retention and organic matter build-up in soils |
| Q30385865 | Soil Functional Zone Management: A Vehicle for Enhancing Production and Soil Ecosystem Services in Row-Crop Agroecosystems. |
| Q46291065 | Soil carbon cycling proxies: Understanding their critical role in predicting climate change feedbacks |
| Q34981025 | Soil microbial community composition does not predominantly determine the variance of heterotrophic soil respiration across four subtropical forests |
| Q34757286 | Soil microbial responses to warming and increased precipitation and their implications for ecosystem C cycling. |
| Q35012294 | Soil warming alters microbial substrate use in alpine soils. |
| Q38189355 | Stoichiometric imbalances between terrestrial decomposer communities and their resources: mechanisms and implications of microbial adaptations to their resources |
| Q42040078 | Stoichiometric plasticity of microbial communities is similar between litter and soil in a tropical rainforest |
| Q57249858 | Stoichiometry of microbial carbon use efficiency in soils |
| Q46931658 | Substrate and environmental controls on microbial assimilation of soil organic carbon: a framework for Earth system models |
| Q36621695 | Synergistic Processing of Biphenyl and Benzoate: Carbon Flow Through the Bacterial Community in Polychlorinated-Biphenyl-Contaminated Soil. |
| Q36012312 | Terrestrial nitrogen cycling in Earth system models revisited |
| Q92281290 | The Polyextremophilic Bacterium Clostridium paradoxum Attains Piezophilic Traits by Modulating Its Energy Metabolism and Cell Membrane Composition |
| Q30978286 | The complex relationship between microbial growth rate and yield and its implications for ecosystem processes |
| Q57069807 | The continuing relevance of “older” mycorrhiza literature: insights from the work of John Laker Harley (1911–1990) |
| Q88664878 | The extent and pathways of nitrogen loss in turfgrass systems: Age impacts |
| Q47191162 | The phosphorus-rich signature of fire in the soil-plant system: a global meta-analysis |
| Q35774441 | The physiology and ecological implications of efficient growth. |
| Q30575585 | The role of plants in the effects of global change on nutrient availability and stoichiometry in the plant-soil system |
| Q91245019 | The role of soil redox conditions in microbial phosphorus cycling in humid tropical forests |
| Q58241683 | The temperature response of soil microbial efficiency and its feedback to climate |
| Q34554207 | Thermal acclimation in widespread heterotrophic soil microbes |
| Q30715852 | Thermal adaptation of decomposer communities in warming soils |
| Q58413399 | Thinning Can Reduce Losses in Carbon Use Efficiency and Carbon Stocks in Managed Forests Under Warmer Climate |
| Q35791958 | Topsoil and Deep Soil Organic Carbon Concentration and Stability Vary with Aggregate Size and Vegetation Type in Subtropical China |
| Q28601657 | Toward a Predictive Understanding of Earth's Microbiomes to Address 21st Century Challenges |
| Q30666399 | Tradeoffs in microbial carbon allocation may mediate soil carbon storage in future climates. |
| Q92358930 | Tropical Rainforest Restoration Plantations Are Slow to Restore the Soil Biological and Organic Carbon Characteristics of Old Growth Rainforest |
| Q30965145 | Two decades of warming increases diversity of a potentially lignolytic bacterial community. |
| Q38767033 | Uncertain future soil carbon dynamics under global change predicted by models constrained by total carbon measurements |
| Q38859337 | Use of 13 C- and phosphate 18 O-labeled substrate for studying phosphorus and carbon cycling in soils: a proof of concept. |