Soil Biology & Biochemistry

Papers
(The TQCC of Soil Biology & Biochemistry is 25. 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 2021-08-01 to 2025-08-01.)
ArticleCitations
Microbial transformation mechanisms of particulate organic carbon to mineral-associated organic carbon at the chemical molecular level: Highlighting the effects of ambient temperature and soil moistur559
A microbial-explicit model with comprehensive nitrogen processes to quantify gaseous nitrogen production from agricultural soils252
Revisiting process-based simulations of soil nitrite dynamics: Tighter cycling between nitrite and nitrate than considered previously192
The soil microbial community and plant biomass differentially contribute to the retention and recycling of urinary-N in grasslands189
Limited effects of century-old biochar on taxonomic and functional diversities of collembolan communities across land-uses185
Drying-rewetting of permanent pasture and agricultural soils induces a shift towards microbial use of more C-rich organic matter167
Biogeography of soil protistan consumer and parasite is contrasting and linked to microbial nutrient mineralization in forest soils at a wide-scale167
Scaling up taxon-specific microbial traits to predict community-level microbial activity in agricultural systems157
Microbial “hotspots” of organic matter decomposition in temperate peatlands are driven by local spatial heterogeneity in abiotic conditions and not by vegetation structure156
Wildland fire ash enhances short-term CO2 flux from soil in a Southern African savannah152
Legacy effects of rhizodeposits on soil microbiomes: A perspective146
Protists modulate fungal community assembly in paddy soils across climatic zones at the continental scale144
Strong rhizosphere priming effects on N dynamics in soils with higher soil N supply capacity: The ‘Matthew effect’ in plant-soil systems141
The influence of soil development on the depth distribution and structure of soil microbial communities138
Impact of common sample pre-treatments on key soil microbial properties133
Responses of root architecture and the rhizosphere microbiome assembly of maize (Zea mays L.) to a soil texture gradient132
Trophic interrelationships drive the biogeography of protistan community in agricultural ecosystems131
Nitrate-induced hydroxyl radical releases deep soil organic carbon by opening the ‘enzyme latch’ under micro-aerobic conditions129
Altered rainfall greatly affects enzyme activity but has limited effect on microbial biomass in Australian dryland soils127
Carbon acquisition ecological strategies to connect soil microbial biodiversity and carbon cycling126
Abundant and rare fungal taxa exhibit different patterns of phylogenetic niche conservatism and community assembly across a geographical and environmental gradient123
Recoupling C and N cycles: a fertiliser template to synchronise N supply and limit C priming?118
Stability of iron-carbon complexes determines carbon sequestration efficiency in iron-rich soils117
Editorial Board113
Tackling global biogeography and drivers of soil microbial dehalogenation traits and taxa: Insights from metagenomic profiling based on a curated dehalogenase database111
Nitrogen induced soil carbon gains are resistant to loss after the cessation of excess nitrogen inputs109
Response of soil microbial diversity and functionality to snow removal in a cool-temperate forest107
Aggregate fractions shaped molecular composition change of soil organic matter in a rice paddy under elevated CO2 and air warming107
Distinct mechanisms drive plant-nitrifier interactions in topsoil and subsoil103
Arbuscular mycorrhizal inoculation and plant response strongly shape bacterial and eukaryotic soil community trajectories100
Tree decline and mortality following pathogen invasion alters the diversity, composition and network structure of the soil microbiome100
Shrub effects on the decomposition microenvironment and changes in litter quality have opposing effects on litter decomposition97
Long-term warming-induced trophic downgrading in the soil microbial food web96
Crop productivity, resource allocation and nitrogen concentration as affected by soil decomposers, mixed cropping and crop genotype96
Multi-amplicon nitrogen cycling gene standard: An innovative approach for quantifying N-transforming soil microbes in terrestrial ecosystems94
Different responses of nitrous oxide emissions to liming and manure amendment of an acidic ultisol are controlled by autotrophic and heterotrophic nitrification91
Soil oxidoreductase zymography: Visualizing spatial distributions of peroxidase and phenol oxidase activities at the root-soil interface91
Cry for help from rhizosphere microbiomes and self-rescue strategies cooperatively alleviate drought stress in spring wheat91
Fungal decomposition and transformation of molecular and colloidal fractions of dissolved organic matter extracted from boreal forest soil90
Phosphorus addition ameliorates soil micro-food web simplification due to nitrogen enrichment but does not restore nematode community composition89
Dual role of silt and clay in the formation and accrual of stabilized soil organic carbon88
Earthworm ecotype diversity mitigates resource limitations of microbial community in arable soils88
Root exudation processes induce the utilization of microbial-derived components by rhizoplane microbiota under conservation agriculture88
Time-dependent regulation of soil aggregates on fertilizer N retention and the influence of straw mulching85
Nitrogen addition altered the plant-arbuscular mycorrhizal fungi network through reducing redundant interactions in an alpine meadow85
VNIR and MIR spectroscopy of PLFA-derived soil microbial properties and associated soil physicochemical characteristics in an experimental plant diversity gradient84
Conversion of SIC to SOC enhances soil carbon sequestration and soil structural stability in alpine ecosystems of the Qinghai-Tibet Plateau84
Soil macrofauna: Study problems and perspectives83
Soil metabolomics - current challenges and future perspectives82
Comparative analysis of diversity and environmental niches of soil bacterial, archaeal, fungal and protist communities reveal niche divergences along environmental gradients in the Alps82
Metabolic pathways of CO2 fixing microorganisms determined C-fixation rates in grassland soils along the precipitation gradient82
Straw return and low N addition modify the partitioning of dissimilatory nitrate reduction by increasing conversion to ammonium in paddy fields80
From rhizosphere to detritusphere – Soil structure formation driven by plant roots and the interactions with soil biota80
Biochar addition regulates soil and earthworm gut microbiome and multifunctionality79
Earthworms in an enhanced weathering mesocosm experiment: Effects on soil carbon sequestration, base cation exchange and soil CO2 efflux78
Drought-induced changes in rare microbial community promoted contribution of microbial necromass C to SOC in a subtropical forest77
Contrasting effects of biological soil crusts on soil respiration in a typical steppe77
Expedited loss of soil biodiversity in blue carbon ecosystems caused by rising sea levels76
Corrigendum to “Spatial and temporal detection of root exudates with a paper-based microfluidic device” [Soil Biol. Biochem. 195 (2024), 109456]76
Hydrophilic and hydrophobic fractions of extracellular fungal phosphatases interact differently with clay mineral surfaces74
Sporadic P limitation constrains microbial growth and facilitates SOM accumulation in the stoichiometrically coupled, acclimating microbe–plant–soil model74
Soil textural control on moisture distribution at the microscale and its effect on added particulate organic matter mineralization73
Enhanced mite grazing leads to pattern shifts in soil N2O emissions after organic fertilizer application73
Selective utilization of organic carbon molecules promotes arsenic methylation by increasing methyltransferase activity in arsM-harboring microbes of paddy soils73
Nitrogen availability and mineral particles contributed fungal necromass to the newly formed stable carbon pool in the alpine areas of Southwest China73
Spatial and temporal detection of root exudates with a paper-based microfluidic device73
Manure application effects on subsoils: Abundant taxa initiate the diversity reduction of rare bacteria and community functional alterations73
Shedding light on the functional role of the Ignavibacteria in Italian rice field soil: A meta-genomic/transcriptomic analysis72
Editorial Board72
Long-term N-addition alters the community structure of functionally important N-cycling soil microorganisms across global grasslands72
Arbuscular mycorrhizal fungi have a greater role than root hairs of maize for priming the rhizosphere microbial community and enhancing rhizosphere organic P mineralization72
The effects of climate warming and exogenous nitrogen input on soil N2O emissions from mangroves72
Addition of base cations increases microbial carbon use efficiency and biomass in acidic soils70
Contrasting responses of microbial diversity and community structure in decaying root bark and xylem to N addition in an alpine shrubland70
Historical forest disturbance reduces soil microbial efficiency across multiple carbon sources69
Resolving dynamic mineral-organic interactions in the rhizosphere by combining in-situ microsensors with plant-soil reactive transport modeling69
The interplay between Azospirillum brasilense and the native bacterial communities in the soil and rhizosphere of maize (Zea mays L.)69
Thermodynamic control on the decomposition of organic matter across different electron acceptors69
No thermal adaptation in soil extracellular enzymes across a temperate grassland region69
Depth effects on bacterial community assembly processes in paddy soils67
Rice root Fe plaque increases paddy soil CH4 emissions via the promotion of electron transfer for syntrophic methanogenesis66
Microbial resistance in rhizosphere hotspots under biodegradable and conventional microplastic amendment: Community and functional sensitivity66
Testing the environmental controls of microbial nitrogen-mining induced by semi-continuous labile carbon additions in the subarctic66
Rapid transfer of C and N excreted by decomposer soil animals to plants and above-ground herbivores66
Pathways of biogenically excreted organic matter into soil aggregates65
Mineral type and land-use intensity control composition and functions of microorganisms colonizing pristine minerals in grassland soils65
Microbial necromass as the source of soil organic carbon in global ecosystems65
Impact of graphite nano amendments on soil enzyme activities, functional genes and microbiome composition in a soil-plant system65
Coupling energy balance and carbon flux during cellulose degradation in arable soils64
Eukaryotes in soil aggregates across conservation managements: Major roles of protists, fungi and taxa linkages in soil structuring and C stock64
Carbon flow from roots to rhizobacterial networks: Grafting effects64
Energy and matter dynamics in an estuarine soil are more sensitive to warming than salinization64
A global meta-analysis reveals the positive effect of invasive alien plants on soil heterotrophic respiration63
Soil carbon mineralization and microbial community dynamics in response to pyrogenic organic matter addition62
Spatial access and resource limitations control carbon mineralization in soils62
Effects of warming on bacterial growth rates in a peat soil under ambient and elevated CO262
Reductive dissolution of iron phosphate modifies rice root morphology in phosphorus-deficient paddy soils61
Identification of the rhizosphere microbes that actively consume plant-derived carbon61
Role of different size classes of organisms in cropped soils: What do litterbag experiments tell us? A meta-analysis60
Whole soil warming promotes surface soil carbon loss but deep soil carbon gain, depending on land management practices in temperate climate59
Alternate wetting-drying had no preferences for rice P uptake but increased microbial P allocation to phospholipids: Evidence from dual 32P and 33P labeling59
Field application of pure polyethylene microplastic has no significant short-term effect on soil biological quality and function59
Mixing with coniferous tree species alleviates rhizosphere soil phosphorus limitation of broad-leaved trees in subtropical plantations59
Drought shifts soil nematodes to smaller size across biological scales57
Kinetics of arsenic and antimony reduction and oxidation in peatlands treating mining-affected waters: Effects of microbes, temperature, and carbon substrate57
Disentangling carbon stabilization in a Calcisol subsoil amended with iron oxyhydroxides: A dual-13C isotope approach56
Soil clay minerals: An overlooked mediator of gross N transformations in Regosolic soils of subtropical montane landscapes56
Root exudation and rhizosphere microbial assembly are influenced by novel plant trait diversity in carrot genotypes56
Organic cropping systems alter metabolic potential and carbon, nitrogen and phosphorus cycling capacity of soil microbial communities55
Abundant and rare bacteria possess different diversity and function in crop monoculture and rotation systems across regional farmland55
A global meta-analysis on freeze-thaw effects on soil carbon and phosphorus cycling55
Plant root exudates and rhizosphere bacterial communities shift with neighbor context55
Tillage and pesticide seed treatments have distinct effects on soil microbial diversity and function54
Editorial Board54
Altered microbial CAZyme families indicated dead biomass decomposition following afforestation54
Primary carbon sources and self-induced metabolic landscapes shape community structure in soil bacterial hotspots54
Editorial Board54
Modeling ecosystem-scale carbon dynamics in soil: The microbial dimension53
Molecular weight of dissolved organic matter determines its interactions with microbes and its assembly processes in soils53
Soil P availability and mycorrhizal type determine root exudation in sub-tropical forests53
Alterations in substrate stoichiometry control the responses of soil diazotrophs to nutrient enrichment52
Disproportional oxidation rates of ammonia and nitrite deciphers the heterogeneity of fertilizer-induced N2O emissions in agricultural soils51
Dynamic changes in bacterial community structure are associated with distinct priming effect patterns51
Microbial community assembly and its influencing factors of secondary forests in Qinling Mountains51
Priming effect varies with root order: A case of Cunninghamia lanceolata50
Divergent responses of soil glomalin and microbial necromass to precipitation reduction: New perspectives from soil aggregates and multi-trophic networks50
Soil nematode community profiling using reference-free mito-metagenomics49
Do chromogenic assays of soil enzyme activities need buffers? More disadvantages than advantages of modified universal buffer in the para-nitrophenyl-based assay of phosphomonoesterase and β-glucosida49
Forest restoration increases energy flow through the fungal channel and decreases energy flow through the herbivorous channel in soil micro-food webs49
Corrigendum to “Plant phenology modulates and undersown cover crops mitigate N2O emissions” [Soil Biol. Biochem. 198 (2024) 109548]49
Rewetting alongside biochar and sulphate addition mitigates greenhouse gas emissions and retain carbon in degraded upland peatlands48
Spatiotemporal variation in soil methane uptake in a cool-temperate immature deciduous forest48
Simplified estimates of soil nematode body mass using maximum diameter: Insights from large-scale grasslands across China48
Transferring concepts from plant to microbial ecology: A framework proposal to identify relevant bacterial functional traits48
Factors predictive of the biogeographic distribution of comammox Nitrospira in terrestrial ecosystems48
Tillage homogenizes soil bacterial communities in microaggregate fractions by facilitating dispersal47
How does organic amendment affect soil microbial nitrate immobilization rate?47
Regulation of soil nitrogen cycling by shrubs in grasslands47
Nitrifier controls on soil NO and N2O emissions in three chaparral ecosystems under contrasting atmospheric N inputs46
Fiddler crab bioturbation stimulates methane emissions in mangroves: Insights into microbial mechanisms46
Soil microbial response to silicate fertilization reduces bioavailable arsenic in contaminated paddies46
Dominant plants affect litter decomposition mainly through modifications of the soil microbial community45
Rice rhizodeposition promotes the build-up of organic carbon in soil via fungal necromass45
Evaluation of the relation between soil biomass of arbuscular mycorrhizal fungi and glomalin-related soil protein in conservation agriculture45
Litter diversity accelerates labile carbon but slows recalcitrant carbon decomposition45
Priming effect on soil carbon decomposition by root exudate surrogates: A meta-analysis45
Phosphorus limitation regulates the responses of microbial carbon metabolism to long-term combined additions of nitrogen and phosphorus in a cropland45
Dynamic stability of mineral-associated organic matter: enhanced stability and turnover through organic fertilization in a temperate agricultural topsoil45
Editorial Board44
Corrigendum to “A meta-analysis of global cropland soil carbon change from cover cropping” [Soil Biol. Biochem. 143 (2020) 107735]44
Editorial Board44
Nematode community diversity and function across an alpine landscape undergoing plant colonization of previously unvegetated soils43
Editorial Board43
Interplanting leguminous shrubs boosts the trophic interactions of soil micro-food web in a karst grassland43
Structure and function of bacterial metaproteomes across biomes43
The only constant is change: Endogenous circadian rhythms of soil microbial activities43
The soil microbial methylome: A tool to explore the role of epigenetic memory in driving soil abiotic legacy effects43
Linking Rock-Eval parameters to soil heterotrophic respiration and microbial residues in a black soil42
Earthworm influence on soil aggregate distribution and protected carbon at managed forest sites in Vermont, USA42
Plant organ rather than cover crop species determines residue incorporation into SOC pools41
N-induced soil acidification triggers metal stimulation of soil methane oxidation in a temperate steppe ecosystem41
Nitrogen addition increases the glucose-induced priming effect of the particulate but not the mineral-associated organic carbon fraction41
Differential accumulation patterns of microbial necromass induced by maize root vs. shoot residue addition in agricultural Alfisols41
When microclimates meet soil microbes: Temperature controls soil microbial diversity along an elevational gradient in subtropical forests41
Plant mixture effects on carbon-degrading enzymes promote soil organic carbon accumulation41
Aeolian dust deposition as a driver of cyanobacterial community structure in biological soil crusts40
Carbon cycle in the microbial ecosystems of biological soil crusts40
Topographic differences in nitrogen cycling mediate nitrogen retention in a subtropical, N-saturated forest catchment40
Deciphering factors controlling decay and nitrogen accumulation in coarse wood debris of five tree species using 15N labeled wood disks40
Microplastics exert minor influence on bacterial community succession during the aging of earthworm (Lumbricus terrestris) casts40
Preceding crop legacy modulates the early growth of winter wheat by influencing root growth dynamics, rhizosphere processes, and microbial interactions40
High stochasticity in rare bacterial community assembly in rice-wheat rotation soils at a regional scale39
Precipitation balances deterministic and stochastic processes of bacterial community assembly in grassland soils39
Acidic amelioration of soil amendments improves soil health by impacting rhizosphere microbial assemblies39
Distinct seasonal and annual variability of prokaryotes, fungi and protists in cropland soil under different tillage systems and soil texture39
Restructuring of soil food webs reduces carbon storage potential in boreal peatlands39
Co-localised phosphorus mobilization processes in the rhizosphere of field-grown maize jointly contribute to plant nutrition39
Visualizing the transfer of organic matter from decaying plant residues to soil mineral surfaces controlled by microorganisms39
Degradation dynamics and microbial processes in yak dung on the Tibetan Plateau39
Elevated CO2 and nitrogen interactively affect the rhizosphere priming effect of Cunninghamia lanceolata39
Editorial Board38
D genome acquisition and breeding have had a significant impact on interaction of wheat with ACC deaminase producers in soil or ACC deaminase potential activity in the rhizosphere38
Editorial Board38
Obituary : Clive Arthur Tudor Edwards - 16 June 1925–20 July 202138
Editorial Board38
Seed treatment with plant-defense elicitors decreases the abundance of ammonia oxidizers associated with winter wheat roots38
Editorial Board38
Editorial Board38
Nitrogen-15 natural abundance is robust to quantify nitrogen transfer from clover to grass in temporary grassland38
Long-term N inputs shape microbial communities more strongly than current-year inputs in soils under 10-year continuous corn cropping37
Tracing sources and turnover of soil organic matter in a long-term irrigated dry forest using a novel hydrogen isotope approach37
Distinct N-cycling microbial communities contribute to microtopographic variation in soil N2O emissions from denitrification37
The role of the soil microbiome in the colonisation of glacier forefields by Antarctic pearlwort (Colobanthus quitensis) under current and future climate change scenarios37
Wood decomposition in poorly-drained forested wetland soils: How important are termites?37
Adult body mass influences multi-element stoichiometry in ground beetles37
Seasonal changes in soil biofilm microbial communities37
Specific utilization of biopolymers of plant and fungal origin reveals the existence of substrate-specific guilds for bacteria in temperate forest soils37
Disentangling the abiotic and biotic components of AMF suppressive soils36
Phosphorus fertiliser source determines the allocation of root-derived organic carbon to soil organic matter fractions36
Deepened snow in combination with summer warming increases growing season nitrous oxide emissions in dry tundra, but not in wet tundra36
Aridity thresholds of microbiome-soil function relationship along a climatic aridity gradient in alpine ecosystem35
Aligning theoretical and empirical representations of soil carbon-to-nitrogen stoichiometry with process-based terrestrial biogeochemistry models35
Global climate changes decoupled soil nitrogen mineralization and immobilization35
Biocrusts drive soil respiration across seasons and depths in a cold-winter desert35
Linkages between the temperature sensitivity of soil respiration and microbial life strategy are dependent on sampling season35
The effects of tree-mycorrhizal type on soil organic matter properties from neighborhood to watershed scales35
Bacterial community response to environmental change varies with depth in the surface soil35
Lithologic control of microbial-derived carbon in forest soils35
Nitrogen deposition stimulates decomposition via changes in the structure and function of litter food webs35
Polar soils exhibit distinct patterns in microbial diversity and dominant phylotypes35
Decoupled responses of leaf and root decomposition to nutrient deposition in a subtropical plantation35
Shifts in C-degradation genes and microbial metabolic activity with vegetation types affected the surface soil organic carbon pool35
Contributions of microbial necromass and plant lignin to soil organic carbon stock in a paddy field under simulated conditions of long-term elevated CO2 and warming35
The influence of forest-to-cropland conversion on temperature sensitivity of soil microbial respiration across tropical to temperate zones35
Iron oxidation coupled with nitrate reduction affects the acetate-assimilating microbial community structure elucidated by stable isotope probing in flooded paddy soil35
Obituary: Philip Charles Brookes: 26th March 1951–28th September 202334
Soil microbial communities are driven by the declining availability of cations and phosphorus during ecosystem retrogression34
Respiration and carbon use efficiency characteristics of soluble protein-derived carbon by soil microorganisms: A case study at afforested sites34
Opposite priming responses to labile carbon versus oxygen pulses in anoxic peat34
Interactive dynamics between rhizosphere bacterial and viral communities facilitate soybean fitness to cadmium stress revealed by time-series metagenomics34
Land use intensification homogenizes soil protist communities and alters their diversity across Europe34
Editorial Board34
Insight into the role of competition in niche differentiation between ammonia-oxidizing archaea and bacteria in ammonium-rich alkaline soil: A network-based study34
Influences of arsenate and/or phosphate adsorption to ferrihydrite on iron-reducing and arsenic-reducing microbial communities in paddy soil revealed by rRNA-13C-acetate probing33
Plants with nitrate preference can regulate nitrification to meet their nitrate demand33
Biocrusts regulate the effect of rainfall pulses on soil respiration at different temporal scales on the Loess Plateau33
A rapid and sensitive assay to quantify amino sugars, neutral sugars and uronic acid necromass biomarkers using pre-column derivatization, ultra-high-performance liquid chromatography and high-resolut33
Use of metabolomics to quantify changes in soil microbial function in response to fertiliser nitrogen supply and extreme drought33
Responses of soil rare and abundant microorganisms to recurring biotic disturbances33
Root exudates from drought-affected plants increase soil respiration across a range of grassland species33
Year-round activity of microbial communities in cold-climate peatlands treating mining-affected waters33
Phosphorus addition decreases soil fungal richness and alters fungal guilds in two tropical forests32
Revising the dynamic energy budget theory with a new reserve mobilization rule and three example applications to bacterial growth32
Plant community composition and traits modulate the impacts of drought intensity on soil microbial community composition and function32
Strong conditionality in plant-fungal community assembly after soil inoculation in post-agricultural grasslands32
Recording earthworm diversity on the tropical island of Martinique using DNA barcoding unveiled endemic species in bromeliad plants32
Physical characterisation of chia mucilage polymeric gel and its implications on rhizosphere science - Integrating imaging, MRI, and modelling to gain insights into plant and microbial amended soils32
Arbuscular mycorrhizal fungal communities of pristine rainforests and adjacent sugarcane fields recruit from different species pools31
Different stochastic processes regulate bacterial and fungal community assembly in estuarine wetland soils31
Dependence of thermal desorption method for profiling volatile organic compound (VOC) emissions from soil31
UV-B stress reshapes root-associated microbial communities and networks, driven by host plant resistance31
Are enzymes transported in soils by water fluxes?31
Increase in iron-bound organic carbon content under simulated sea-level rise: A “marsh organ” field experiment31
Mapping of suitable habitats for earthworms in China31
Divergent belowground carbon allocation patterns of winter wheat shape rhizosphere microbial communities and nitrogen cycling activities31
Rigorous, empirical, and quantitative: a proposed pipeline for soil health assessments31
Soil aggregate isolation method affects interpretation of protistan community31
Time-varying associations between absorptive fine roots and leaf litter decomposition across 23 plant species31
Multitrophic interactions support belowground carbon sequestration through microbial necromass accumulation in dryland biocrusts31
Life at the extreme: Plant-driven hotspots of soil nutrient cycling in the hyper-arid core of the Atacama Desert31
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