Pedobiologia

Papers
(The median citation count of Pedobiologia is 2. 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 2020-04-01 to 2024-04-01.)
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 Plateau16
Functional shifts of soil microbial communities associated with Alliaria petiolata invasion15
Simulated nitrogen deposition decreases soil microbial diversity in a semiarid grassland, with little mediation of this effect by mowing14
Significant effects on soil microbial communities were not detected after strategic tillage following 44 years of conventional or no-tillage management14
Validation and extension of the Tea Bag Index to collect decomposition data from termite-rich ecosystems13
Responses of oribatid mites to warming in boreal peatlands depend on fen type13
The magnitude and direction of priming were driven by soil moisture and temperature in a temperate forest soil of China13
Composition and interaction frequencies in soil bacterial communities change in association with urban park age in Beijing12
Benefits of dual inoculation with arbuscular mycorrhizal fungi and rhizobia on Phaseolus vulgaris planted in a low-fertility tropical soil12
Impact of soil nitrogen availability and pH on tropical heath forest organic matter decomposition and decomposer activity12
Ecological restoration methods influence the structure of arbuscular mycorrhizal fungal communities in degraded drylands11
Stability of soil organic carbon during forest conversion is more sensitive in deep soil than in topsoil in subtropical forests11
Native arbuscular mycorrhizal fungi respond to rehabilitation in iron ore mining areas from the Eastern Brazilian Amazon11
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
Spatial and temporal patterns in soil organic carbon, microbial biomass and activity under different land-use types in a long-term soil-monitoring network11
Nematode grazing increases the allocation of plant-derived carbon to soil bacteria and saprophytic fungi, and activates bacterial species of the rhizosphere10
Decreased burrowing activity of endogeic earthworms and effects on water infiltration in response to an increase in soil bulk density10
Topography is more important than forest type as a determinant for functional trait composition of Collembola community9
Salinity changes root occupancy by arbuscular mycorrhizal fungal species9
Evolutionary terrestrialization scenarios for soil invertebrates9
Variability of arbuscular mycorrhizal fungal communities within the root systems of individual plants is high and influenced by host species and root phosphorus9
Tuber pseudohimalayense ascomata-compartments strongly select their associated bacterial microbiome from nearby pine forest soils independently of their maturation stage9
Shifting prokaryotic communities along a soil formation chronosequence and across soil horizons in a South Taiga ecosystem8
Crop residues in corn-wheat rotation in a semi-arid region increase CO2 efflux under conventional tillage but not in a no-tillage system8
Using X-ray microtomography to characterize the burrowing behaviour of earthworms in heterogeneously polluted soils8
Soil properties and climate affect arbuscular mycorrhizal fungi and soil microbial communities in Mediterranean rainfed cereal cropping systems8
Winter cover crops and no till management enhance enzyme activities in soybean field soils8
Land management drives dynamic changes to microbial function through edaphic factors and soil biota8
Irrigation and fertilization effects on arbuscular mycorrhizal fungi depend on growing season in a dryland maize agroecosystem8
Metabarcoding mites: Three years of elevated CO2 has no effect on oribatid assemblages in a Eucalyptus woodland8
Litter inputs drive increases in topsoil organic carbon after scrub encroachment in an alpine grassland7
Nitrogen enrichment affects soil enzymatic stoichiometry via soil acidification in arid and hot land7
Tools for monitoring and study of peregrine pheretimoid earthworms (Megascolecidae)7
Nematode contributions to the soil food web trophic structure of two contrasting boreal peatlands in Canada7
Amazonian deforestation and its influence on soil biotic factors and abiotic properties7
Earthworms did not increase long-term nitrous oxide fluxes in perennial forage and riparian buffer ecosystems6
Metaproteomes reveal increased capacity for stress tolerance of soil microbes in ferruginous tropical rocky outcrops6
Soil environment influences plant growth-promotion traits of isolated rhizobacteria6
Soil and microbial nutrient status are heterogeneous within an elevational belt on a neotropical mountain6
Dynamics of soil microarthropod populations affected by a combination of extreme climatic events in tropical home gardens of Kerala, India5
Soil fauna groups respond differentially to changes in crop rotation cycles in rice production systems5
Bar-HRM for identification of cryptic earthworm species5
Belowground plant-plant signaling of root infection by nematodes5
Tuber aestivum is associated with changes in soil chemistry and reduced biological quality in a Quercus pubescens stand in Northern Italy5
Response of soil biodiversity to global change5
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-dwelling arthropods as indicators of erosion in a South African grassland habitat5
Trophic groups of soil fauna in semiarid: Impacts of land use change, climatic seasonality and environmental variables4
Salinization causes abrupt reduction in soil nematode abundance in the Caatinga area of the Submedio San Francisco Valley, Brazilian semiarid region4
Shade affects fine-root morphology in range-encroaching eastern redcedars (Juniperus virginiana) more than competition, soil fertility and pH4
Impact of legumes on soil microbial activity and C cycle functions in two contrasting Cameroonian agro-ecological zones4
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
Soil microbial community dynamics indicate disruption of nitrogen cycling by pollution in vegetation buffer zones4
Stramenopiles and Cercozoa dominate the heterotrophic protist community of biological soil crusts irrespective of edaphic factors4
Differential effects of nutrient addition and woody plant encroachment on grassland soil, litter and plant dynamics across a precipitation gradient4
High-throughput sequencing and conventional morphotyping show different soil nematode assemblages but similar community responses to altitudinal gradients on Mt. Ibuki, Japan4
Bacterial and fungal communities, but not physicochemical properties, of soil differ according to root rot status of pea4
Determination of litter derived C and N in litterbags and soil using stable isotopes prevents overestimation of litter decomposition in alley cropping systems4
Forest plantations reduce soil functioning in terrestrial ecosystems from South Africa4
Distribution of physiochemically defined soil organic carbon pools and their relationship to the soil microbial community in grasslands4
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
Nature development in degraded landscapes: How pioneer bioturbators and water level control soil subsidence, nutrient chemistry and greenhouse gas emission4
Abundance, isolation, and characterization of halotolerant microbes from common oligosaline soils3
Greater impacts of phosphorus fertilization on soil phosphatase activity in tropical forests than in non-tropical natural terrestrial ecosystems: A meta-analysis3
Do local-scale context dependencies shape how ectomycorrhizal fungal diversity structures with reduced or sustained experimental N addition?3
Changes in soil bacterial communities, and carbon and nitrogen metrics as potential indicators of land use effects in a humid tropical forest3
Soil biotic effects and competition; What are the mechanisms behind being a successful invader?3
Does metal pollution affect the stoichiometry of soil-litter food webs?3
Agricultural practices influence biological soil quality indicators in an irrigated semiarid agro-ecosystem3
Earthworms regulate the nematode community by directly enhancing the bacterial-based energy channel rather than through the effect of casts3
Litter thickness and soil pH influence the diversity of saprotrophic fungi in primary forest fragments in the Amazon3
Fast improvement of macrofauna communities and soil quality in plantain crops converted to agroecological practices3
Oribatid (Acari: Oribatida) diversity in natural and altered open arid ecosystems of South-Eastern Caucasus3
Litter decomposition and microbial communities alters depending on litter type and overstory species in revegetated agricultural land3
Plant diversity decreases potential nitrous oxide emissions from restored agricultural soil3
Responses of Collembola communities to mixtures of wheat varieties: A trait-based approach3
Soil macrofaunal activity, microbial catabolic limitations and nutrient cycling in cropping systems amended with woody residues and nitrogen inputs3
Litter arthropods community in multifunctional landscapes: Spatial and temporal complementarity of Brazilian ecosystems3
Contributions of temporal and spatial variation to the diversity of soil-dwelling testate amoeba assemblages in a swampy forest2
Drainage increases species richness and density of soil macro-invertebrates in the Zoige peatland of eastern Tibetan Plateau2
Soil physicochemical properties shape distinct nematode communities in serpentine ecosystems2
Weak effect of plant canopy but strong impact of depth on variation of cultivable microfungal communities through soil profiles in semiarid Spain2
Cover crop selection affects maize susceptibility to the fungal pathogen Fusarium verticillioides2
Variance, locality and structure: Three experimental challenges in the study of the response of soil microbial communities to multiple perturbations2
Revegetation of mined areas influences the physiological profile of bacterial communities and improves the biochemical functions of soil2
Shade tree identity rather than diversity influences soil macrofauna in cacao-based agroforestry systems2
Soil metabolomics reveal complex interactions between Arthrobacter ureafaciens and Trichoderma harzianum when co-inoculated on wheat2
Leaf-cutting ant (Atta cephalotes) nests may be hotspots of methane and carbon dioxide emissions in tropical forests2
A standardized and miniaturized method to investigate rhizosphere microorganisms, with a focus on methanogenic archaea and methanotrophic bacteria2
Mapping the effects of Melinis minutiflora invasion on soil nitrogen dynamics in the Brazilian savanna: A dual-isotope approach2
Bioturbation by dung beetles and termites. Do they similarly impact soil and hydraulic properties?2
Potential of slash-and-mulch system with legumes to conserve soil attributes and macrofauna diversity in Eastern Amazon2
Three-dimensional mapping of earthworm (Lumbricus terrestris) seed transport2
Microbial P limitation in tropical forest soils could be overestimated: Insight from a sorption experiment and a meta-analysis2
Effects of mound building Lasius flavus on organic carbon and nutrient fluxes in soils of temperate grassland ecosystems2
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