Biology and Fertility of Soils

Papers
(The TQCC of Biology and Fertility of Soils is 12. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-05-01 to 2026-05-01.)
ArticleCitations
Low nocturnal temperature changed protected tomato soil bacterial community composition and metabolite characteristics96
Synergistic biogas slurry–wood vinegar application accelerates cotton stalk degradation in saline soil by modulating bacterial network complexity and organic acid metabolism58
Responses of bacterial community composition and diversity to multi-level nitrogen addition at different periods of growing season driven by conditional rare taxa in an alpine meadow53
Manure distribution interacts with soil moisture and nitrate availability in controlling soil N2O emissions53
How arbuscular mycorrhizal fungi maintain plant nitrogen acquisition under drought51
Protists: the hidden ecosystem players in a wetland rice field soil51
Isolation and characterization of Rhizobium from non-leguminous potato plants: New frontiers in Rhizobium research50
Inoculation and tracking of beneficial microbes reveal they can establish in field-grown potato roots and decrease blemish diseases50
Dual-functional Bacillus amyloliquefaciens mediates autotoxin degradation and pathogen suppression in monocropped foxtail millet49
Absolute microbiome profiling highlights the links among microbial stability, soil health, and crop productivity under long-term sod-based rotation46
Root organic acid exudation mediates rhizosphere bacteria dynamics during drought–rehydration in Broussonetia papyrifera45
Restoration of degraded alpine meadows from the perspective of plant–soil feedbacks44
Are lipids, phenylpropanoids, and benzenoids potential metabolite biomarkers for succession in desert biocrusts?43
A shift from nitrification to denitrification-dominated N2O emission in an acidic soil following organic amendment40
Mechanism of increased soil phosphorus availability in a calcareous soil by ammonium polyphosphate39
Correction to: A 5-and a-half-year-experiment shows precipitation thresholds in litter decomposition and nutrient dynamics in arid and semi-arid regions38
Using fluorescence lifetime imaging to disentangle microbes from the heterogeneous soil matrix38
Editorial: Recent advances in biology and fertility studies of paddy field soil38
Exploring polyphosphates in soil: presence, extractability, and contribution to microbial biomass phosphorus35
Organic fertilization drives shifts in microbiome complexity and keystone taxa increase the resistance of microbial mediated functions to biodiversity loss34
Arbuscular mycorrhizal fungi with contrasting life-history strategies differently affect health-promoting compounds in field-grown tomato by changing arbuscule occurrence and mycorrhizal assemblages i34
Correction to: Inter-microbial competition for N and plant NO3- uptake rather than BNI determine soil net nitrification under intensively managed Brachiaria humidicola33
Niche differentiation and higher uptake of available nitrogen maintained the productivity of alpine meadow at early degradation32
Rethinking discrepancies between difference and 15 N methods for estimating fertilizer nitrogen recovery31
Rhizosphere-competent actinobacteria with ACC deaminase activity mitigate heavy metal stress in corn (Zea mays)30
The rhizosphere exhibits higher microbial carbon use efficiency compared to bulk soil30
Dynamic modulation of rhizosphere microbial diversity and function across tobacco growth stages by biochar30
Trunk injection of oxytetracycline improves plant performance and alters the active bark and rhizosphere microbiomes in huanglongbing-affected citrus trees29
Endophytic N2 fixation in sweet potato: responses to N, P, and K inputs and visualization of 15N2 utilizing bacterial cells via Raman spectroscopy28
Bio-organic fertilizer enhances soil mineral solubilization, microbial community stability, and fruit quality in an 8-year watermelon continuous cropping system28
Genotypic richness affects inorganic N uptake and N form preference of a clonal plant via altering soil N pools28
Earthworms promote soil organic carbon formation across management histories without stimulating the mineralization of native carbon26
Microorganisms regulate soil phosphorus fractions in response to low nocturnal temperature by altering the abundance and composition of the pqqC gene rather than that of the phoD gene25
Liming enhances the abundance and stability of nitrogen-cycling microbes: the buffering effect of long-term lime application25
Nitrogen uptake and reallocation from roots drive the regrowth of a dominant plant in temperate grassland after low defoliation25
Phosphorus (P) mobilisation from inorganic and organic P sources depends on P-acquisition strategies in dioecious Populus euphratica25
Shifts in understory plant composition induced by nitrogen addition predict soil fungal beta diversity in a boreal forest25
Effects of nitrogen inputs on soil organic carbon in a subtropical plantation forest: variation with nitrogen addition methodology24
Bacterial necromass determines the response of mineral-associated organic matter to elevated CO224
Organic fertilization strengthens multiple internal pathways for soil mineral nitrogen production: evidence from the meta-analysis of long-term field trials23
Mineral N suppressed priming effect while increasing microbial C use efficiency and N2O production in sandy soils under long-term conservation management23
Interactive effects of plant litter chemistry and organic/inorganic forms of nitrogen addition on Moso bamboo (Phyllostachys edulis) soil respiration22
Nitrate supply increases the resistance of cucumber to Fusarium wilt disease by regulating root exudation22
Restoration of degraded alpine grasslands alters plant–microbial competition for nitrogen22
Soil contribution to the cobalamin (vitamin B12) supply of terrestrial organisms22
Hybrid pathways of denitrification drive N2O but not N2 emissions from an acid-sulphate sugarcane soil21
Unveiling the crucial role of rice root iron plaque in enhancing biological nitrogen fixation via 15N-labeling DNA-SIP and metagenomics in a model study21
Litter complexity rather than land-use intensity emerges as a key driver of taxonomic and isotopic diversity of Collembola in urban systems20
Continuous intake of facade eluates affects active and total soil Microbiome20
Impacts of grazing management on biocrust microbiomes and their potential to input and cycle nutrients20
Linking nitrous oxide emissions and soil urease kinetics with uratolytic microbial communities: effects of nano zero-valent iron and dicyandiamide19
Elevational patterns of microbial carbon use efficiency in a subtropical mountain forest19
Activity of anaerobic methane oxidation driven by different electron acceptors and the relative microbiome in paddy fields across various rice growth periods and soil layers19
Functional redundant soil fauna and microbial groups and processes were fairly resistant to drought in an agroecosystem19
Twenty years of overfertilization with organic materials increased total phosphorus cycling without changing the relative contributions of biotic and abiotic fluxes18
Converting acidic forests to managed plantations reduces soil nitrogen loss by inhibiting autotrophic nitrification while inducing nitrate immobilization in the tropics18
Biological nitrification inhibitors show low persistence in agricultural soils: the role of pH and soil microbiota18
Organic nitrogen fertilization benefits selected soil fauna in global agroecosystems18
Type I methanotrophs dominated methane oxidation and assimilation in rice paddy fields by the consequence of niche differentiation17
Land use types affect soil microbial NO3− immobilization through changed fungal and bacterial contribution in alkaline soils of a subtropical montane agricultural landscape17
Lysis of soil microbial cells by CO2 or N2 high pressurization compared with chloroform fumigation17
Utilisation and transformation of organic and inorganic nitrogen by soil microorganisms and its regulation by excessive carbon and nitrogen availability16
The soil treatment trade-off of didecyl dimethyl ammonium chloride: stimulated nitrogen cycling against a backdrop of impaired carbon metabolism and expanding antibiotic resistance16
Bacteria from the rhizosphere of a selenium hyperaccumulator plant can improve the selenium uptake of a non-hyperaccumulator plant16
Microbial carbon use efficiency of litter with distinct C/N ratios in soil at different temperatures, including microbial necromass as growth component16
Reducing antibiotic resistance genes through biochar-enhanced reductive soil disinfestation16
Herbivore Dung inputs mainly drive copiotrophic bacterial contributions to soil nutrient pool turnover in alpine grasslands15
Spotting ethylene in forest soils—What influences the occurrence of the phytohormone?15
Microbial and isotopomer analysis of N2O production pathways in a calcareous film-mulched farmland15
Root-associated microbiome dynamics reveal ecological responses to soil-borne pathogens in susceptible and tolerant tobacco varieties15
Increasing phosphorus availability reduces priming effect by facilitating microbial carbon use efficiency in a subtropical forest soil15
Investigating protistan predators and bacteria within soil microbiomes in agricultural ecosystems under organic and chemical fertilizer applications15
A 5-and a-half-year-experiment shows precipitation thresholds in litter decomposition and nutrient dynamics in arid and semi-arid regions15
Competition between shrubs and grasses in a shrub‒encroached temperate grassland: Implications from nitrogen acquisition15
How to adequately represent biological processes in modeling multifunctionality of arable soils15
Hysteretic response of N2O reductase activity to soil pH variations after application of lime to an acidic agricultural soil14
Grassland above- and below-ground inputs have similar effects on soil organic matter: A five-year field trial14
Phosphate-solubilizing inoculants induce stage-specific rhizosphere microbiome shifts and enhance chickpea symbiosis under low P availability14
Response of acetochlor degradation and bacterial community in black soil to the application of vermicompost14
Divergent effects of straw and biochar on soil carbon priming are depth-dependent in subtropical Moso bamboo forests14
Nitrogen additions increase soil microbial nitrate- rather than ammonium- immobilization14
Harnessing key bacteria from suppressive soil to mitigate banana Panama disease14
Responses of soil carbon and nutrient cycling to global change and human disturbances in forest ecosystems14
Effect of no-till followed by crop diversification on the soil microbiome in a boreal short cereal rotation13
Effects of organic mulching on soil aggregates, main microbial groups, and enzyme activity in Chinese hickory plantation13
Nitrous oxide fluxes, their sources, and soil microbial communities depend more on carbon availability than long- and short-term phosphorus addition13
Grazing exclusion increases soil organic C through microbial necromass of root-derived C as traced by 13C labelling photosynthate13
pH thresholds govern the effects of catechol on some C-related enzyme activities under contrasting hydrological regimes13
Biochar reshapes soil bacterial community composition and survival strategies: a meta-analysis revealing trade-offs between microbial stability and functional complexity13
Pyrolysis temperature affects biochar suitability as an alternative rhizobial carrier13
Fixation of CO2 by soil fungi: contribution to organic carbon pool and destination of fixed carbon products12
A 13C-PLFA approach to assess the crop carbon allocation efficiency and arbuscular mycorrhizal assimilation capacity under conservation tillage12
Soil bacterial and fungal communities beneath different forest types differentially and promptly respond to non-catastrophic typhoon disturbance12
Mulching increases soil organic carbon via plant inputs and its microbial transformation12
Alkalization solution affects selectivity of absorbance for colorimetric quantification of para-nitrophenol in soil enzyme activity assays12
Contrasting fine root-induced rhizosphere priming effects between coniferous and broadleaved trees12
N2O production is influenced by the abundance of nitrite-reducers and N2O-reducers in casts produced by a large variety of tropical earthworm species12
Effect of agricultural management system (“cash crop”, “livestock” and “climate optimized”) on nitrous oxide and ammonia emissions12
Root hair-deficient mutant of maize promoted an increase in C and N in loamy soil after 5 years of monoculture12
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