Pedobiologia

Papers
(The TQCC of Pedobiologia is 4. 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 2020-02-01 to 2024-02-01.)
ArticleCitations
Response of soil fauna to simulated global change factors depends on ambient climate conditions24
Climate and soil properties regulate soil fungal communities on the Loess Plateau14
Responses of oribatid mites to warming in boreal peatlands depend on fen type13
Significant effects on soil microbial communities were not detected after strategic tillage following 44 years of conventional or no-tillage management13
Simulated nitrogen deposition decreases soil microbial diversity in a semiarid grassland, with little mediation of this effect by mowing13
The magnitude and direction of priming were driven by soil moisture and temperature in a temperate forest soil of China12
Impact of soil nitrogen availability and pH on tropical heath forest organic matter decomposition and decomposer activity12
Benefits of dual inoculation with arbuscular mycorrhizal fungi and rhizobia on Phaseolus vulgaris planted in a low-fertility tropical soil12
Ecological restoration methods influence the structure of arbuscular mycorrhizal fungal communities in degraded drylands11
Composition and interaction frequencies in soil bacterial communities change in association with urban park age in Beijing11
Spatial and temporal patterns in soil organic carbon, microbial biomass and activity under different land-use types in a long-term soil-monitoring network11
Stability of soil organic carbon during forest conversion is more sensitive in deep soil than in topsoil in subtropical forests11
Increases in substrate availability and decreases in soil pH drive the positive effects of nitrogen addition on soil net nitrogen mineralization in a temperate meadow steppe11
Validation and extension of the Tea Bag Index to collect decomposition data from termite-rich ecosystems11
Nematode grazing increases the allocation of plant-derived carbon to soil bacteria and saprophytic fungi, and activates bacterial species of the rhizosphere10
Move or change, an eco-evolutionary dilemma: The case of Collembola10
Salinity changes root occupancy by arbuscular mycorrhizal fungal species9
Variability of arbuscular mycorrhizal fungal communities within the root systems of individual plants is high and influenced by host species and root phosphorus9
Decreased burrowing activity of endogeic earthworms and effects on water infiltration in response to an increase in soil bulk density9
Metabarcoding mites: Three years of elevated CO2 has no effect on oribatid assemblages in a Eucalyptus woodland8
Topography is more important than forest type as a determinant for functional trait composition of Collembola community8
Crop residues in corn-wheat rotation in a semi-arid region increase CO2 efflux under conventional tillage but not in a no-tillage system8
Native arbuscular mycorrhizal fungi respond to rehabilitation in iron ore mining areas from the Eastern Brazilian Amazon8
Shifting prokaryotic communities along a soil formation chronosequence and across soil horizons in a South Taiga ecosystem8
Tuber pseudohimalayense ascomata-compartments strongly select their associated bacterial microbiome from nearby pine forest soils independently of their maturation stage8
Winter cover crops and no till management enhance enzyme activities in soybean field soils8
Using X-ray microtomography to characterize the burrowing behaviour of earthworms in heterogeneously polluted soils8
Evolutionary terrestrialization scenarios for soil invertebrates8
Tools for monitoring and study of peregrine pheretimoid earthworms (Megascolecidae)7
Irrigation and fertilization effects on arbuscular mycorrhizal fungi depend on growing season in a dryland maize agroecosystem7
Nematode contributions to the soil food web trophic structure of two contrasting boreal peatlands in Canada7
Soil and microbial nutrient status are heterogeneous within an elevational belt on a neotropical mountain6
Nitrogen enrichment affects soil enzymatic stoichiometry via soil acidification in arid and hot land6
Earthworms did not increase long-term nitrous oxide fluxes in perennial forage and riparian buffer ecosystems6
Soil environment influences plant growth-promotion traits of isolated rhizobacteria6
Metaproteomes reveal increased capacity for stress tolerance of soil microbes in ferruginous tropical rocky outcrops6
Soil properties and climate affect arbuscular mycorrhizal fungi and soil microbial communities in Mediterranean rainfed cereal cropping systems6
Influence of understory vegetation on soil bacterial communities and nitrogen cycling gene abundance in cool-temperate and sub-alpine forests along an elevational gradient5
Soil fauna groups respond differentially to changes in crop rotation cycles in rice production systems5
Consistent effects of a non-native earthworm on soil microbial communities in three subtropical forests5
Dynamics of soil microarthropod populations affected by a combination of extreme climatic events in tropical home gardens of Kerala, India5
Land management drives dynamic changes to microbial function through edaphic factors and soil biota5
Bar-HRM for identification of cryptic earthworm species5
Tolerance of testate amoeba species to rising sea levels under laboratory conditions and in the South Pacific5
Soil-dwelling arthropods as indicators of erosion in a South African grassland habitat5
Shade affects fine-root morphology in range-encroaching eastern redcedars (Juniperus virginiana) more than competition, soil fertility and pH4
Fire effects on biochemical properties of a semiarid pine forest topsoil at cm-scale4
Effects of defoliation frequencies on above- and belowground biodiversity and ecosystem processes in subtropical grasslands of southern Brazil4
Bacterial and fungal communities, but not physicochemical properties, of soil differ according to root rot status of pea4
Trophic groups of soil fauna in semiarid: Impacts of land use change, climatic seasonality and environmental variables4
Stramenopiles and Cercozoa dominate the heterotrophic protist community of biological soil crusts irrespective of edaphic factors4
Amazonian deforestation and its influence on soil biotic factors and abiotic properties4
High-throughput sequencing and conventional morphotyping show different soil nematode assemblages but similar community responses to altitudinal gradients on Mt. Ibuki, Japan4
Litter inputs drive increases in topsoil organic carbon after scrub encroachment in an alpine grassland4
Communities of Collembola show functional resilience in a long-term field experiment simulating climate change4
Invasive earthworms Amynthas tokioensis and Amynthas agrestis alter macronutrients (Ca, Mg, K, P) in field and laboratory forest soils4
Distribution of physiochemically defined soil organic carbon pools and their relationship to the soil microbial community in grasslands4
Tuber aestivum is associated with changes in soil chemistry and reduced biological quality in a Quercus pubescens stand in Northern Italy4
Impact of legumes on soil microbial activity and C cycle functions in two contrasting Cameroonian agro-ecological zones4
Response of soil biodiversity to global change4
Nature development in degraded landscapes: How pioneer bioturbators and water level control soil subsidence, nutrient chemistry and greenhouse gas emission4
Soil microbial community dynamics indicate disruption of nitrogen cycling by pollution in vegetation buffer zones4
Forest plantations reduce soil functioning in terrestrial ecosystems from South Africa4
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