| Soil quality - A critical review |
181 |
| Exposure of soil collembolans to microplastics perturbs their gut microbiota and alters their isotopic composition |
56 |
| The role of nitrifier denitrification in the production of nitrous oxide revisited |
52 |
| Nitrification and nitrifiers in acidic soils |
50 |
| Decreasing soil microbial diversity is associated with decreasing microbial biomass under nitrogen addition |
45 |
| A meta-analysis of soil extracellular enzyme activities in response to global change |
45 |
| Isolating organic carbon fractions with varying turnover rates in temperate agricultural soils - A comprehensive method comparison |
36 |
| Greatest soil microbial diversity found in micro-habitats |
36 |
| Rhizosphere size and shape: Temporal dynamics and spatial stationarity |
35 |
| Antibiotic resistance genes and associated bacterial communities in agricultural soils amended with different sources of animal manures |
34 |
| Soil pH correlates with the co-occurrence and assemblage process of diazotrophic communities in rhizosphere and bulk soils of wheat fields |
34 |
| Rare taxa of alkaline phosphomonoesterase-harboring microorganisms mediate soil phosphorus mineralization |
33 |
| Long-term manure application increases soil organic matter and aggregation, and alters microbial community structure and keystone taxa |
33 |
| Ecoenzymatic stoichiometry and microbial nutrient limitation in rhizosphere soil in the arid area of the northern Loess Plateau, China |
31 |
| Soil organic carbon stocks in topsoil and subsoil controlled by parent material, carbon input in the rhizosphere, and microbial-derived compounds |
30 |
| The root of the matter: Linking root traits and soil organic matter stabilization processes |
30 |
| Responses of soil microbial community to continuous experimental nitrogen additions for 13 years in a nitrogen-rich tropical forest |
27 |
| Microbial growth and carbon use efficiency in soil: Links to fungal-bacterial dominance, SOC-quality and stoichiometry |
26 |
| Niche separation of comammox Nitrospira and canonical ammonia oxidizers in an acidic subtropical forest soil under long-term nitrogen deposition |
25 |
| Microbial competition for nitrogen and carbon is as intense in the subsoil as in the topsoil |
25 |
| Root litter decomposition slows with soil depth |
24 |
| Effect of nitrogen fertilization on the abundance of nitrogen cycling genes in agricultural soils: A meta-analysis of field studies |
24 |
| Organic amendments increase crop yields by improving microbe-mediated soil functioning of agroecosystems: A meta-analysis |
24 |
| Microbial stoichiometric flexibility regulates rice straw mineralization and its priming effect in paddy soil |
24 |
| The ratio of Gram-positive to Gram-negative bacterial PLFA markers as an indicator of carbon availability in organic soils |
24 |
| Nitrous oxide emissions and biogeochemical responses to soil freezing-thawing and drying-wetting |
24 |
| Clarifying the interpretation of carbon use efficiency in soil through methods comparison |
23 |
| Biochar reduces soil heterotrophic respiration in a subtropical plantation through increasing soil organic carbon recalcitrancy and decreasing carbon degrading microbial activity |
23 |
| Phosphate levels influence the utilisation of rice rhizodeposition carbon and the phosphate-solubilising microbial community in a paddy soil |
23 |
| Soil microbial biomass size and soil carbon influence the priming effect from carbon inputs depending on nitrogen availability |
22 |
| Wheat rhizosphere harbors a less complex and more stable microbial co-occurrence pattern than bulk soil |
22 |
| Long-term fertilization influences community assembly processes of soil diazotrophs |
22 |
| Growth explains microbial carbon use efficiency across soils differing in land use and geology |
22 |
| Review and synthesis of the effects of elevated atmospheric CO2 on soil processes: No changes in pools, but increased fluxes and accelerated cycles |
21 |
| Comammox Nitrospira clade B contributes to nitrification in soil |
21 |
| A comparison of the ability of PLFA and 16S rRNA gene metabarcoding to resolve soil community change and predict ecosystem functions |
21 |
| Alive and kicking: Why dormant soil microorganisms matter |
21 |
| Structure and assembly cues for rhizospheric nirK- and nirS-type denitrifier communities in long-term fertilized soils |
20 |
| Linking organic matter chemistry with soil aggregate stability: Insight from C-13 NMR spectroscopy |
20 |
| Cover cropping and no-till increase diversity and symbiotroph:saprotroph ratios of soil fungal communities |
20 |
| Microbial extracellular polymeric substances improve water retention in dryland biological soil crusts |
20 |
| Variation in microbial community structure correlates with heavy-metal contamination in soils decades after mining ceased |
19 |
| Winter soil freeze-thaw cycles lead to reductions in soil microbial biomass and activity not compensated for by soil warming |
19 |
| Dissimilatory nitrate reduction to ammonium (DNRA), not denitrification dominates nitrate reduction in subtropical pasture soils upon rewetting |
19 |
| Impact of long-term agricultural management practices on soil prokaryotic communities |
19 |
| Responses of fungal-bacterial community and network to organic inputs vary among different spatial habitats in soil |
19 |
| Long-term fertilisation form, level and duration affect the diversity, structure and functioning of soil microbial communities in the field |
18 |
| Litter species richness and composition effects on fungal richness and community structure in decomposing foliar and root litter |
18 |
| Co-occurrence patterns of soybean rhizosphere microbiome at a continental scale |
18 |
| Conservation agriculture practices increase soil microbial biomass carbon and nitrogen in agricultural soils: A global meta-analysis |
18 |
