Soil Biology & Biochemistry

Papers
(The median citation count of Soil Biology & Biochemistry is 9. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
Soil viral community dynamics over seven years of heat disturbance: Spatial variation exceeds temporal in annually sampled soils610
Microbial carbon use efficiency of mineral-associated organic matter is related to its desorbability448
Adult body mass influences multi-element stoichiometry in ground beetles419
Comparing plant litter molecular diversity assessed from proximate analysis and 13C NMR spectroscopy220
Tree species-dependent effects of urbanization and plant invasion on deadwood biota and decomposition rates211
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 warming178
Cropping system modulates the effect of spring drought on ammonia-oxidizing communities174
Termite bioturbation: Fungal versus non-fungal building strategies lead to different soil sheeting stability157
Tree species richness increases spatial variation but not overall wood decomposition156
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Obituary142
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Termite graveyards. Hidden geochemical patches?113
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Obituary : Clive Arthur Tudor Edwards - 16 June 1925–20 July 2021111
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Abundant and rare fungal taxa exhibit different patterns of phylogenetic niche conservatism and community assembly across a geographical and environmental gradient109
Dual isotopic (33P and 18O) tracing and solution 31P NMR spectroscopy to reveal organic phosphorus synthesis in organic soil horizons107
Nitrogen addition slows litter decomposition accompanied by accelerated manganese release: A five-year experiment in a subtropical evergreen broadleaf forest107
Oxygen gas derived oxygen does not affect the accuracy of 18O-labelled water approach for microbial carbon use efficiency106
Niche differentiation of bacteria and fungi in carbon and nitrogen cycling of different habitats in a temperate coniferous forest: A metaproteomic approach104
The unexplored role of preferential flow in soil carbon dynamics104
Increasing plant species diversity enhances microbial necromass carbon content but does not alter its contribution to soil organic carbon pool in a subtropical forest100
Global climate changes decoupled soil nitrogen mineralization and immobilization99
Evidence for a genetic basis in functional trait tradeoffs with microbial growth rate but not growth yield96
Pasture-crop rotations modulate the soil and rhizosphere microbiota and preserve soil structure supporting oat cultivation in the Pampa biome96
Warming shifts the biomass distribution of soil microarthropod communities95
The path less taken: Long-term N additions slow leaf litter decomposition and favor the physical transfer pathway of soil organic matter formation90
Response of soil organic carbon decomposition to intensified water variability co-determined by the microbial community and aggregate changes in a temperate grassland soil of northern China90
Normalizing time in terms of space: What drives the fate of spring thaw-released nitrogen in a sloping Arctic landscape?89
Iron oxidation coupled with nitrate reduction affects the acetate-assimilating microbial community structure elucidated by stable isotope probing in flooded paddy soil89
Strong rhizosphere priming effects on N dynamics in soils with higher soil N supply capacity: The ‘Matthew effect’ in plant-soil systems88
Distribution of phosphorus cycling genes across land uses and microbial taxonomic groups based on metagenome and genome mining88
Earthworms as conveyors of mycorrhizal fungi in soils84
Amino acid isotopes in functional assemblages of Collembola reveal the influence of vertical resource heterogeneity and root energy supply on trophic interactions in soil food webs84
Depth-dependent driver of global soil carbon turnover times83
A pulse of simulated root exudation alters the composition and temporal dynamics of microbial metabolites in its immediate vicinity82
A meta-analysis of phosphatase activity in agricultural settings in response to phosphorus deficiency81
Revegetation promotes soil mineral-associated organic carbon sequestration and soil carbon stability in the Tengger Desert, northern China79
Ephemeral microbial responses to pulses of bioavailable carbon in oxic and anoxic salt marsh soils77
Soil nutrient conditions alter viral lifestyle strategy and potential function in phosphorous and nitrogen metabolisms76
Stabilized microbial necromass in soil is more strongly coupled with microbial diversity than the bioavailability of plant inputs76
Litter mixture effects on nitrogen dynamics during decomposition predominantly vary among biomes but little with litter identity, diversity and soil fauna76
Tracing sources and turnover of soil organic matter in a long-term irrigated dry forest using a novel hydrogen isotope approach75
Susceptibility of new soil organic carbon to mineralization during dry-wet cycling in soils from contrasting ends of a precipitation gradient75
Differential effects of soil trophic networks on microbial decomposition activity in mountain ecosystems74
Phosphorus fertiliser source determines the allocation of root-derived organic carbon to soil organic matter fractions74
Adaptation of soil micro-food web to elemental limitation: evidence from the forest-steppe ecotone73
Top-down effects on biological soil crust function72
Biogeography of soil protistan consumer and parasite is contrasting and linked to microbial nutrient mineralization in forest soils at a wide-scale72
Will a legacy of enhanced resource availability accelerate the soil microbial response to future climate change?72
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Distinct N-cycling microbial communities contribute to microtopographic variation in soil N2O emissions from denitrification70
Deepened snow in combination with summer warming increases growing season nitrous oxide emissions in dry tundra, but not in wet tundra69
Mitigating generative AI inaccuracies in soil biology69
Testing microbial models with data from a 14C glucose tracer experiment69
Aridity thresholds of microbiome-soil function relationship along a climatic aridity gradient in alpine ecosystem68
A microbial-explicit model with comprehensive nitrogen processes to quantify gaseous nitrogen production from agricultural soils68
Aridity and NPP constrain contribution of microbial necromass to soil organic carbon in the Qinghai-Tibet alpine grasslands67
Short-term soil fungal community dynamics following fire in mediterranean climate-type banksia woodlands67
Investigating drivers of free-living diazotroph activity in paddy soils across China67
Plant litter traits control microbial decomposition and drive soil carbon stabilization66
Microbial substrate stoichiometry governs nutrient effects on nitrogen cycling in grassland soils66
Wildland fire ash enhances short-term CO2 flux from soil in a Southern African savannah66
Mosses stimulate soil carbon and nitrogen accumulation during vegetation restoration in a humid subtropical area65
Global prediction of soil microbial growth rates and carbon use efficiency based on the metabolic theory of ecology65
Biochar application differentially affects soil micro-, meso-macro-fauna and plant productivity within a nature restoration grassland65
Shaping of soil microbial communities by plants does not translate into specific legacy effects on organic carbon mineralization64
Impact of common sample pre-treatments on key soil microbial properties64
Disentangling the abiotic and biotic components of AMF suppressive soils64
Importance of microbial communities at the root-soil interface for extracellular polymeric substances and soil aggregation in semiarid grasslands63
Protists modulate fungal community assembly in paddy soils across climatic zones at the continental scale63
Spatially-distributed microbial enzyme activities at intact, coated macropore surfaces in Luvisol Bt-horizons62
Trophic interrelationships drive the biogeography of protistan community in agricultural ecosystems62
Measurements of fine root decomposition rate: Method matters61
Within-species plant phylogeny drives ectomycorrhizal fungal community composition in tree roots along a timberline60
Polar soils exhibit distinct patterns in microbial diversity and dominant phylotypes60
Seasonality drives microbiome composition and nitrogen cycling in soil below biocrusts60
Nitrogen limitation of microbial activity in alpine tundra soils along an environmental gradient: Intra-seasonal variations and effect of rising temperature60
Bacterial community response to environmental change varies with depth in the surface soil59
Functional trait variation and community-weighted means of tree traits can alter soil microbial biomass and community composition59
The soil microbial community and plant biomass differentially contribute to the retention and recycling of urinary-N in grasslands59
N2 fixation per unit microbial biomass increases with aridity59
Increase of temperature exacerbates the conversion of P fractions in organic horizon58
Mycorrhizal fungi-mediated uptake of tree-derived nutrients by crops – the role of tree-maintained versus crop-associated fungal mycelia58
Poly(L-lactide) mineralisation under environmental conditions is enhanced in earthworm guts57
The influence of forest-to-cropland conversion on temperature sensitivity of soil microbial respiration across tropical to temperate zones57
Dominant herbaceous plants contribute to the spatial heterogeneity of beech and riparian forest soils by influencing fungal and bacterial diversity57
Number of global change factors alters plant-soil feedbacks via its effect on soil fungal communities57
Fourteen-year field experiment reveals neutral effects of N and P deposition on abundance and stoichiometric traits of the earthworm Pontoscolex corethrurus in tropical plantations57
Phase transformation of schwertmannite changes microbial iron and sulfate-reducing processes in flooded paddy soil and decreases arsenic accumulation in rice (Oryza sativa L.)56
A rhizosphere effect promotes the persistence of gas oxidization activity in soil55
Spatial substrate heterogeneity limits microbial growth as revealed by the joint experimental quantification and modeling of carbon and heat fluxes55
Soil bacterial and fungal communities show within field heterogeneity that varies by land management and distance metric55
Virome responses to heating of a forest soil suggest that most dsDNA viral particles do not persist at 90°C55
Are carbon-storing soils more sensitive to climate change? A laboratory evaluation for agricultural temperate soils54
Scaling up taxon-specific microbial traits to predict community-level microbial activity in agricultural systems54
Altered rainfall greatly affects enzyme activity but has limited effect on microbial biomass in Australian dryland soils54
Soil fungal community and mating type development of Tuber melanosporum in a 20-year chronosequence of black truffle plantations53
Methane flux from transplanted soil monoliths depends on moisture, but not origin53
Opportunities and limits in imaging microorganisms and their activities in soil microhabitats53
The effects of cadmium-copper stress on the accumulation of antibiotic-resistance genes in soil and pakchoi leaves52
An optimised molecular-based method for ecological study of tardigrades in soils52
Biological denitrification inhibition (BDI) on nine contrasting soils: An unexpected link with the initial soil denitrifying community52
Study of soil heterotrophic respiration as a function of soil moisture under different land covers52
Effect of rice (Oryza sativa L.) genotype on yield: Evidence from recruiting spatially consistent rhizosphere microbiome51
Nitrate-induced hydroxyl radical releases deep soil organic carbon by opening the ‘enzyme latch’ under micro-aerobic conditions51
Experimental evidence that poor soil phosphorus (P) solubility typical of drylands due to calcium co-precipitation favors autonomous plant P acquisition over collaboration with mycorrhizal fungi51
Tree species richness and N-fixing tree species enhance the chemical stability of soil organic carbon in subtropical plantations51
The role of the soil microbiome in the colonisation of glacier forefields by Antarctic pearlwort (Colobanthus quitensis) under current and future climate change scenarios51
What drives leaf litter decomposition and the decomposer community in subtropical forests – The richness of the above-ground tree community or that of the leaf litter?51
The effects of tree-mycorrhizal type on soil organic matter properties from neighborhood to watershed scales50
Root traits explain multitrophic interactions of belowground microfauna on soil nitrogen mineralization and plant productivity50
Organic and inorganic sulfur and nitrogen uptake by co-existing grassland plant species competing with soil microorganisms50
Arbuscular mycorrhizal fungi associated with alpine meadow multifunctionality in a warmer climate with variable precipitation50
Deepened snow cover accelerates litter decomposition by stimulating microbial degradation49
Long-term N inputs shape microbial communities more strongly than current-year inputs in soils under 10-year continuous corn cropping49
Rhizosphere effects of woody plants on soil biogeochemical processes: A meta-analysis48
Nitrogen-15 natural abundance is robust to quantify nitrogen transfer from clover to grass in temporary grassland48
Anaerobic oxidation of methane mitigates net methane production and responds to long-term experimental warming in a northern bog48
Vegetation transition from meadow to forest reduces priming effect on SOM decomposition48
No effect of long-term soil warming on diffusive soil inorganic and organic nitrogen fluxes in a temperate forest soil48
Seed treatment with plant-defense elicitors decreases the abundance of ammonia oxidizers associated with winter wheat roots48
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 rhizosphere47
Threats to the soil microbiome from nanomaterials: A global meta and machine-learning analysis47
Deepened snow enhances gross nitrogen cycling among Pan-Arctic tundra soils during both winter and summer47
Revisiting process-based simulations of soil nitrite dynamics: Tighter cycling between nitrite and nitrate than considered previously47
Responses of root architecture and the rhizosphere microbiome assembly of maize (Zea mays L.) to a soil texture gradient47
Soluble phenols in litter are reduced during passage through the soil macrofauna gut due to the formation of insoluble complexes with proteins: A case study with isopods and Diptera larvae47
Corrigendum to “Nitrite-dependent anaerobic oxidation decreases methane emissions from peatlands” [Soil Biology and Biochemistry 169, 108658]46
Life in the dark: Impact of future winter warming scenarios on carbon and nitrogen cycling in Arctic soils46
Land use intensification homogenizes soil protist communities and alters their diversity across Europe46
Gross N transformations and plant N use efficiency in intensive vegetable production soils46
Corrigendum to “Impact of nitrogen addition on plant-soil-enzyme C–N–P stoichiometry and microbial nutrient limitation” [Soil Biol. Biochem. 170 (2022) 108714]45
Rice root Fe plaque enhances oxidation of microbially available organic carbon via Fe(III) reduction-coupled microbial respiration45
Biocrusts drive soil respiration across seasons and depths in a cold-winter desert45
Soil bacterial community functions and distribution after mining disturbance45
Biochar strategy for long-term N2O emission reduction: Insights into soil physical structure and microbial interaction45
Lithologic control of microbial-derived carbon in forest soils44
Canonical ammonia oxidizers, rather than comammox Nitrospira, dominated autotrophic nitrification during the mineralization of organic substances in two paddy soils44
Impact of grassland afforestation with contrasting tree species on soil phosphorus fractions and alkaline phosphatase gene communities44
The positive role of root decomposition on the bioremediation of organic pollutants contaminated soil: A case study using PCB-9 as a model compound44
Organic amendments, deficit irrigation, and microbial communities impact extracellular polysaccharide content in agricultural soils44
Keystone bacterial functional module activates P-mineralizing genes to enhance enzymatic hydrolysis of organic P in a subtropical forest soil with 5-year N addition43
Iron–organic carbon associations stimulate carbon accumulation in paddy soils by decreasing soil organic carbon priming43
The importance of rare versus abundant phoD-harboring subcommunities in driving soil alkaline phosphatase activity and available P content in Chinese steppe ecosystems43
Microbial community dynamics during decomposition of insect exuviae and frass in soil43
Seasonal changes in soil biofilm microbial communities42
Microbial organic matter reduction regulates methane and carbon dioxide production across an ombrotrophic-minerotrophic peatland gradient42
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 moistur42
Decoupled responses of leaf and root decomposition to nutrient deposition in a subtropical plantation42
Sequestration of soil carbon by burying it deeper within the profile: A theoretical exploration of three possible mechanisms41
The spatial distribution of soil microbial necromass affects nutrient mobilization and beech nutrition on silicate and calcareous forest soils41
Phosphorus-mediated succession of microbial nitrogen, carbon, and sulfur functions in rice-driven saline-alkali soil remediation41
Microbial “hotspots” of organic matter decomposition in temperate peatlands are driven by local spatial heterogeneity in abiotic conditions and not by vegetation structure41
The nitrogen gap in soil health concepts and fertility measurements41
Long-term regional evidence of the effects of livestock grazing on soil microbial community structure and functions in surface and deep soil layers40
Aligning theoretical and empirical representations of soil carbon-to-nitrogen stoichiometry with process-based terrestrial biogeochemistry models40
Carbon acquisition ecological strategies to connect soil microbial biodiversity and carbon cycling39
Phosphorus - A key element determining nitrous oxide emissions from boreal cultivated peat soil39
Increased soil organic carbon response to fertilization is associated with increasing microbial carbon use efficiency: Data synthesis39
Belowground responses to altered precipitation regimes in two semi-arid grasslands39
Biochar with large specific surface area recruits N2O-reducing microbes and mitigate N2O emission39
Invasive Spartina alterniflora accelerates soil gross nitrogen transformations to optimize its nitrogen acquisition in an estuarine and coastal wetland of China39
Forest dieback switches the relationships between microfaunal bacterivore guilds and soil nutrients39
Earthworms facilitate stabilization of both more-available maize biomass and more-recalcitrant maize biochar on mineral particles in an agricultural soil39
Dynamics of root–microbe interactions governing crop phosphorus acquisition after straw amendment38
Limited effects of century-old biochar on taxonomic and functional diversities of collembolan communities across land-uses38
Casing soil microbiome mediates suppression of bacterial blotch of mushrooms during consecutive cultivation cycles38
Stoichiometric imbalance and microbial community regulate microbial elements use efficiencies under nitrogen addition38
Resistance of microbial community and its functional sensitivity in the rhizosphere hotspots to drought38
Globally nitrogen addition alters soil microbial community structure, but has minor effects on soil microbial diversity and richness38
Energy flux across multitrophic levels drives ecosystem multifunctionality: Evidence from nematode food webs37
Response of soil microbial communities to mixed beech-conifer forests varies with site conditions37
Arbuscular mycorrhizal fungi and goethite promote carbon sequestration via hyphal-aggregate mineral interactions37
Nitrogen deposition stimulates decomposition via changes in the structure and function of litter food webs37
Intercropping with legumes alleviates soil N limitation but aggravates P limitation in a degraded agroecosystem as shown by ecoenzymatic stoichiometry37
The influence of soil development on the depth distribution and structure of soil microbial communities36
How the Birch effect differs in mechanisms and magnitudes due to soil texture36
Chronic enhanced nitrogen deposition and elevated precipitation jointly benefit soil microbial community in a temperate forest36
Altered litter stoichiometry drives energy dynamics of food webs through changing multiple facets of soil biodiversity36
Invasive plant-derived dissolved organic matter alters microbial communities and carbon cycling in soils36
From diversity to complexity: Microbial networks in soils35
The mechanisms underpinning microbial resilience to drying and rewetting – A model analysis35
Specific utilization of biopolymers of plant and fungal origin reveals the existence of substrate-specific guilds for bacteria in temperate forest soils35
Drying-rewetting of permanent pasture and agricultural soils induces a shift towards microbial use of more C-rich organic matter35
Legacy effects of rhizodeposits on soil microbiomes: A perspective34
A synthesis of soil organic carbon mineralization in response to biochar amendment34
Effects of microplastics on plant growth and arbuscular mycorrhizal fungal communities in a soil spiked with ZnO nanoparticles34
Estimating the temperature optima of soil priming34
New insights into the patterns of ecoenzymatic stoichiometry in soil and sediment34
Heterotrophic nitrification – An eternal mystery in the nitrogen cycle34
Direction and magnitude of the change in water content between two periods influence soil respiration, microbial biomass and nutrient availability which can be modified by intermittent air-drying34
Linkages between the temperature sensitivity of soil respiration and microbial life strategy are dependent on sampling season34
Shifts in C-degradation genes and microbial metabolic activity with vegetation types affected the surface soil organic carbon pool33
Decadal application of mineral fertilizers alters the molecular composition and origins of organic matter in particulate and mineral-associated fractions33
Preferential use of organic acids over sugars by soil microbes in simulated root exudation33
Can moisture affect temperature dependences of microbial growth and respiration?33
Higher free-living N2 fixation at rock-soil interfaces than topsoils during vegetation recovery in karst soils33
Drought accentuates the role of mycorrhiza in phosphorus uptake33
Soil fauna actively change their diet to survive stress32
Earthworms in an enhanced weathering mesocosm experiment: Effects on soil carbon sequestration, base cation exchange and soil CO2 efflux32
Clover increases N2O emissions in boreal leys during winter32
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2D distribution of Pseudomonas fluorescens activities at the soil-root interface of sunflower grown on vineyard soils: Effects on copper uptake32
Revising the dynamic energy budget theory with a new reserve mobilization rule and three example applications to bacterial growth32
Arbuscular mycorrhizal fungal diversity in agricultural fields is explained by the historical proximity to natural habitats32
Magnetic enzyme-mimetic minerals with peroxidase-like activity can contribute to measured soil peroxidase activity32
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Recording earthworm diversity on the tropical island of Martinique using DNA barcoding unveiled endemic species in bromeliad plants32
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Arbuscular mycorrhizal fungal communities of pristine rainforests and adjacent sugarcane fields recruit from different species pools32
High trait diversity among soil arthropods allows their survival in a heterogeneous eco-agricultural mosaic32
Long-term warming-induced trophic downgrading in the soil microbial food web31
Humidity controls soil organic carbon accrual in grassland on the Qinghai–Tibet Plateau31
Priming is frequently overestimated in studies using 14C-labelled substrates due to underestimation of 14CO2 activity31
Crop productivity, resource allocation and nitrogen concentration as affected by soil decomposers, mixed cropping and crop genotype31
Conversion of SIC to SOC enhances soil carbon sequestration and soil structural stability in alpine ecosystems of the Qinghai-Tibet Plateau31
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Corrigendum to “Input of high-quality litter reduces soil carbon losses due to priming in a subtropical pine forest” [Soil Biology and Biochemistry 194 (2024) 109444]31
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Obituary: Philip Charles Brookes: 26th March 1951–28th September 202330
Effects of copper contamination on N cycling microbial guilds and plant performance in two contrasting grassland soils30
Rigorous, empirical, and quantitative: a proposed pipeline for soil health assessments30
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-resolut30
Dodder parasitism limited the effect of arbuscular mycorrhizal fungi on litter decomposition30
Plant roots are more strongly linked to microorganisms in leaf litter rather than in soil across tropical land-use systems30
Circum-Arctic peat soils resist priming by plant-derived compounds30
Stability of iron-carbon complexes determines carbon sequestration efficiency in iron-rich soils30
Manganese indicates root decomposition rates across soil layer, root order, and tree species: Evidence from a subtropical forest30
Moisture effects on microbial protein biosynthesis from ammonium and nitrate in an unfertilised grassland30
Divergent responses of soil microorganisms to throughfall exclusion across tropical forest soils driven by soil fertility and climate history29
Niche construction by two ectomycorrhizal truffle species (Tuber aestivum and T. melanosporum)29
Mechanisms behind high N2O emissions from livestock enclosures in Kenya revealed by dual-isotope and functional gene analyses29
Use of metabolomics to quantify changes in soil microbial function in response to fertiliser nitrogen supply and extreme drought29
Drought mediates the response of soil fungal communities post-wildfire in a Californian grassland and coastal sage scrubland29
Rhizosphere microbial communities explain positive effects of diverse crop rotations on maize and soybean performance29
Tree decline and mortality following pathogen invasion alters the diversity, composition and network structure of the soil microbiome29
Arbuscular mycorrhizal inoculation and plant response strongly shape bacterial and eukaryotic soil community trajectories29
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 soils29
Opposite priming responses to labile carbon versus oxygen pulses in anoxic peat28
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