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Effects of Earthworms on the Microbiomes and Antibiotic Resistomes of Detritus Fauna and Phyllospheres
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00374-003-0614-5openalex-snapshot
Earthworms and pH affect communities of nematodes and enchytraeids in forest soil
inferredcites →https://doi.org/10.1007/s00442-009-1374-1openalex-snapshot
Earthworm and belowground competition effects on plant productivity in a plant diversity gradient
inferredcites →https://doi.org/10.1007/s13593-014-0269-7openalex-snapshot
Earthworm services for cropping systems. A review
inferredcites →https://doi.org/10.1016/j.apsoil.2010.04.005openalex-snapshot
Effects of earthworms on above- and belowground herbivores
inferredcites →https://doi.org/10.1016/j.ejsobi.2007.08.015openalex-snapshot
The quality of exogenous organic matter: Short-term influence on earthworm abundance
inferredcites →https://doi.org/10.1016/j.ejsobi.2009.06.001openalex-snapshot
Earthworms enhance plant regrowth in a grassland plant diversity gradient
inferredcites →https://doi.org/10.1016/j.envint.2016.03.026openalex-snapshot
Long-term field application of sewage sludge increases the abundance of antibiotic resistance genes in soil
inferredcites →https://doi.org/10.1016/j.envint.2017.10.016openalex-snapshot
Review of antibiotic resistance in China and its environment
inferredcites →https://doi.org/10.1016/j.scitotenv.2018.07.260openalex-snapshot
Long-term organic fertilization increased antibiotic resistome in phyllosphere of maize
inferredcites →https://doi.org/10.1016/j.scitotenv.2018.12.445openalex-snapshot
The gut microbiota of soil organisms show species-specific responses to liming
inferredcites →https://doi.org/10.1016/j.scitotenv.2019.04.104openalex-snapshot
Effects of diet on gut microbiota of soil collembolans
inferredcites →https://doi.org/10.1016/j.soilbio.2008.06.010openalex-snapshot
Detritivorous earthworms directly modify the structure, thus altering the functioning of a microdecomposer food web
inferredcites →https://doi.org/10.1016/j.soilbio.2010.09.010openalex-snapshot
Movement response of Collembola to the excreta of two earthworm species: Importance of ammonium content and nitrogen forms
inferredcites →https://doi.org/10.1016/j.soilbio.2014.07.011openalex-snapshot
The effect of earthworms ( Lumbricus rubellus ) and simulated tillage on soil organic carbon in a long-term microcosm experiment
inferredcites →https://doi.org/10.1016/j.soilbio.2018.01.015openalex-snapshot
Effect of biochar amendment on the alleviation of antibiotic resistance in soil and phyllosphere of Brassica chinensis L.
inferredcites →https://doi.org/10.1016/j.soilbio.2018.03.011openalex-snapshot
Earthworms differentially modify the microbiome of arable soils varying in residue management
inferredcites →https://doi.org/10.1016/j.soilbio.2018.06.017openalex-snapshot
Feeding behaviour of epi-anecic earthworm species and their impacts on soil microbial communities
inferredcites →https://doi.org/10.1016/j.soilbio.2018.12.015openalex-snapshot
Effects of long-term fertilization on the associated microbiota of soil collembolan
inferredcites →https://doi.org/10.1016/j.still.2018.10.016openalex-snapshot
Rhizosphere interactions between earthworms and arbuscular mycorrhizal fungi increase nutrient availability and plant growth in the desertification soils
inferredcites →https://doi.org/10.1016/s0038-0717(01)00049-9openalex-snapshot
Interaction of the earthworm Diplocardia mississippiensis (Megascolecidae) with microbial and nutrient dynamics in a subtropical Spodosol
inferredcites →https://doi.org/10.1016/s1473-3099(13)70318-9openalex-snapshot
Antibiotic resistance—the need for global solutions
inferredcites →https://doi.org/10.1021/acs.est.7b01420openalex-snapshot
Application of Struvite Alters the Antibiotic Resistome in Soil, Rhizosphere, and Phyllosphere
inferredcites →https://doi.org/10.1021/acs.est.7b04292openalex-snapshot
Antibiotics Disturb the Microbiome and Increase the Incidence of Resistance Genes in the Gut of a Common Soil Collembolan
inferredcites →https://doi.org/10.1021/acs.est.8b02825openalex-snapshot
Exposure of a Soil Collembolan to Ag Nanoparticles and AgNO3Disturbs Its Associated Microbiota and Lowers the Incidence of Antibiotic Resistance Genes in the Gut
inferredcites →https://doi.org/10.1021/acs.est.8b05116openalex-snapshot
Land Use Influences Antibiotic Resistance in the Microbiome of Soil Collembolans Orchesellides sinensis
inferredcites →https://doi.org/10.1038/545030bopenalex-snapshot
Restore earthworms to rebuild topsoil
inferredcites →https://doi.org/10.1038/ismej.2011.139openalex-snapshot
An improved Greengenes taxonomy with explicit ranks for ecological and evolutionary analyses of bacteria and archaea
inferredcites →https://doi.org/10.1038/ismej.2015.253openalex-snapshot
Assembly of the Caenorhabditis elegans gut microbiota from diverse soil microbial environments
inferredcites →https://doi.org/10.1038/nbt.2676openalex-snapshot
Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences
inferredcites →https://doi.org/10.1038/ncomms12151openalex-snapshot
Host genotype and age shape the leaf and root microbiomes of a wild perennial plant
inferredcites →https://doi.org/10.1038/nmeth.f.303openalex-snapshot
QIIME allows analysis of high-throughput community sequencing data
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.270openalex-snapshot
Continental-scale pollution of estuaries with antibiotic resistance genes
inferredcites →https://doi.org/10.1038/nrmicro3399openalex-snapshot
What is a resistance gene? Ranking risk in resistomes
inferredcites →https://doi.org/10.1038/s41396-017-0020-xopenalex-snapshot
Microbial community assembly in wild populations of the fruit fly Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.1222743110openalex-snapshot
Diverse and abundant antibiotic resistance genes in Chinese swine farms
inferredcites →https://doi.org/10.1078/0031-4056-00169openalex-snapshot
Interactions between Eisenia andrei (Oligochaeta) and nematode populations during vermicomposting
inferredcites →https://doi.org/10.1080/11263504.2017.1338627openalex-snapshot
Earthworm effect on root morphology in a split root system
inferredcites →https://doi.org/10.1093/bioinformatics/btp636openalex-snapshot
PyNAST: a flexible tool for aligning sequences to a template alignment
inferredcites →https://doi.org/10.1093/bioinformatics/btq461openalex-snapshot
Search and clustering orders of magnitude faster than BLAST
inferredcites →https://doi.org/10.1093/nar/gku1201openalex-snapshot
rrnDB: improved tools for interpreting rRNA gene abundance in bacteria and archaea and a new foundation for future development
inferredcites →https://doi.org/10.1094/mpmi-10-14-0334-fiopenalex-snapshot
The Plant Microbiome at Work
inferredcites →https://doi.org/10.1097/mpg.0000000000001605openalex-snapshot
Microbiota, Environment, and Diet
inferredcites →https://doi.org/10.1111/1365-2656.12660openalex-snapshot
Nitrogen deposition cancels out exotic earthworm effects on plant‐feeding nematode communities
inferredcites →https://doi.org/10.1111/1462-2920.12712openalex-snapshot
The effect of anthropogenic arsenic contamination on the earthworm microbiome
inferredcites →https://doi.org/10.1111/1755-0998.12645openalex-snapshot
Identifying the plant‐associated microbiome across aquatic and terrestrial environments: the effects of amplification method on taxa discovery
inferredcites →https://doi.org/10.1111/ele.12301openalex-snapshot
Individuals' diet diversity influences gut microbial diversity in two freshwater fish (threespine stickleback and Eurasian perch)
inferredcites →https://doi.org/10.1111/gcb.14003openalex-snapshot
Human dissemination of genes and microorganisms in Earth's Critical Zone
inferredcites →https://doi.org/10.1111/j.1654-1103.2003.tb02228.xopenalex-snapshot
VEGAN, a package of R functions for community ecology
inferredcites →https://doi.org/10.1186/s40168-018-0469-5openalex-snapshot
Low-abundant bacteria drive compositional changes in the gut microbiota after dietary alteration
inferredcites →https://doi.org/10.1371/journal.pone.0009490openalex-snapshot
FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
inferredcites →https://doi.org/10.18520/cs/v113/i06/1064-1071openalex-snapshot
Role of Earthworm in Improving Soil Structure and Functioning
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4797133openalex-extracted
Coevolution of Antibiotic Resistance Genes and Virulence Factor Genes as a Bottleneck of Their Removal in Electricity-Intensified Constructed Wetlands
inferred← citeshttps://doi.org/10.1007/s00253-024-13326-9openalex-snapshot
Department-specific patterns of bacterial communities and antibiotic resistance in hospital indoor environments
inferred← citeshttps://doi.org/10.1007/s42832-026-0445-0openalex-snapshot
Soil macrofauna mucus bacterial community: Insights from cultured earthworms and snails
inferred← citeshttps://doi.org/10.1016/j.agee.2025.110062openalex-snapshot
Phyllosphere to soil: How long-term fencing reshapes grassland microbial community construction and the functional genes
inferred← citeshttps://doi.org/10.1016/j.apsoil.2021.104250openalex-snapshot
Long-term combined application of chemical fertilizers and organic manure shapes the gut microbial diversity and functional community structures of earthworms
inferred← citeshttps://doi.org/10.1016/j.apsoil.2023.104837openalex-snapshot
Exploring the interaction between agronomic practices and soil characteristics on the presence of antibiotic resistance genes in soil
inferred← citeshttps://doi.org/10.1016/j.cej.2025.162765openalex-snapshot
Role of earthworms and their excretion products in reducing antimicrobial resistance and putative pathogens during vermicomposting
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130998openalex-snapshot
Effects of nano- or microplastic exposure combined with arsenic on soil bacterial, fungal, and protistan communities
inferred← citeshttps://doi.org/10.1016/j.coche.2025.101181openalex-snapshot
Microplastics and antibiotics in agricultural soil: mechanisms and implications of co-contamination
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112643openalex-snapshot
How can fertilization regimes and durations shape earthworm gut microbiota in a long-term field experiment?
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118890openalex-snapshot
Antibiotic resistance genes in the animal manure-amended soil-plant system: Occurrence, transmission, bacterial hosts, and human health risks
inferred← citeshttps://doi.org/10.1016/j.envint.2021.106502openalex-snapshot
Vertical distribution of antibiotic resistance genes in an urban green facade
inferred← citeshttps://doi.org/10.1016/j.envint.2021.106703openalex-snapshot
Insights into the roles of fungi and protist in the giant panda gut microbiome and antibiotic resistome
inferred← citeshttps://doi.org/10.1016/j.envint.2023.107903openalex-snapshot
Phyllosphere antibiotic resistome in a natural primary vegetation across a successional sequence after glacier retreat
inferred← citeshttps://doi.org/10.1016/j.envint.2023.108374openalex-snapshot
Dissemination of antibiotic resistance genes through soil-plant-earthworm continuum in the food production environment
inferred← citeshttps://doi.org/10.1016/j.envint.2024.108688openalex-snapshot
Assembly and succession of the phyllosphere microbiome and nutrient-cycling genes during plant community development in a glacier foreland
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109414openalex-snapshot
Polyvinyl chloride microplastic triggers bidirectional transmission of antibiotic resistance genes in soil-earthworm systems
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.119516openalex-snapshot
Effects of soil protists on the antibiotic resistome under long term fertilization
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120900openalex-snapshot
Application of earthworm and silicon can alleviate antibiotic resistance in soil-Chinese cabbage system with ARGs contamination
inferred← citeshttps://doi.org/10.1016/j.gee.2024.07.007openalex-snapshot
Antibiotics-heavy metals combined pollution in agricultural soils: Sources, fate, risks, and countermeasures
inferred← citeshttps://doi.org/10.1016/j.jece.2026.125319openalex-snapshot
Mechanisms and risk control strategies for mitigation of antibiotic resistance genes in livestock manure by earthworm vermicomposting
inferred← citeshttps://doi.org/10.1016/j.jenvman.2025.125562openalex-snapshot
Earthworms attenuate antibiotic resistance genes and mobile genetic elements during vermicomposting of sewage sludge
inferred← citeshttps://doi.org/10.1016/j.jes.2021.04.004openalex-snapshot
Combined pollution of arsenic and Polymyxin B enhanced arsenic toxicity and enriched ARG abundance in soil and earthworm gut microbiotas
inferred← citeshttps://doi.org/10.1016/j.jes.2025.09.065openalex-snapshot
Soil science research in Research Center for Eco-Environmental Sciences: Review and outlook
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.125847openalex-snapshot
Polystyrene microplastics impact the occurrence of antibiotic resistance genes in earthworms by size-dependent toxic effects
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.126018openalex-snapshot
Arsenic bioaccumulation in the soil fauna alters its gut microbiome and microbial arsenic biotransformation capacity
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.127252openalex-snapshot
Oral azoxystrobin driving the dynamic change in resistome by disturbing the stability of the gut microbiota of Enchytraeus crypticus
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.128286openalex-snapshot
Quantitative relationship between earthworms’ sensitivity to organic pollutants and the contaminants’ degradation in soil: A meta-analysis
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.128442openalex-snapshot
Climate warming increases the proportions of specific antibiotic resistance genes in natural soil ecosystems
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131026openalex-snapshot
Exposure to cypermethrin pesticide disturbs the microbiome and disseminates antibiotic resistance genes in soil and the gut of Enchytraeus crypticus
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.132732openalex-snapshot
Network complexity of bacterial community driving antibiotic resistome in the microbiome of earthworm guts under different land use patterns
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.133319openalex-snapshot
Selective enrichment of virulence factor genes in the plastisphere under antibiotic and heavy metal pressures
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134749openalex-snapshot
Removal of intracellular and extracellular antibiotic resistance genes and virulence factor genes using electricity-intensified constructed wetlands
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135525openalex-snapshot
Efficient elimination of antibiotics and antibiotic resistance genes in hyperthermophilic sludge composting
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138681openalex-snapshot
Pivotal role of earthworm gut protists in mediating antibiotic resistance genes under microplastic and sulfamethoxazole stress in soil–earthworm systems
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141205openalex-snapshot
Effects of earthworms on soil virus-associated ARGs and resistance phenotypes in long-term field cropping systems
inferred← citeshttps://doi.org/10.1016/j.jwpe.2025.109262openalex-snapshot
Biochar-based filtration of treated wastewater effectively removes trimethoprim but may introduce antimicrobial resistance determinants over time
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.140409openalex-snapshot
Enhanced removal of ciprofloxacin and reduction of antibiotic resistance genes by earthworm Metaphire vulgaris in soil
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.149337openalex-snapshot
Incubation trial indicated the earthworm intestinal bacteria as promising biodigestor for mitigating tetracycline resistance risk in anthropogenic disturbed forest soil
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.150279openalex-snapshot
Responses of earthworm Metaphire vulgaris gut microbiota to arsenic and nanoplastics contamination
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.150781openalex-snapshot
Attenuation of antibiotic resistance genes in livestock manure through vermicomposting via Protaetia brevitarsis and its fate in a soil-vegetable system
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152851openalex-snapshot
Diverse antibiotic resistance genes and potential pathogens inhabit in the phyllosphere of fresh vegetables
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.154739openalex-snapshot
Dispersal of antibiotic resistance genes in an agricultural influenced multi-branch river network
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.155088openalex-snapshot
Distinct aggregate stratification of antibiotic resistome in farmland soil with long-term manure application
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Combined effects of micro-/nano-plastics and oxytetracycline on the intestinal histopathology and microbiome in zebrafish (Danio rerio)
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Enantioselective effect of the chiral fungicide tebuconazole on the microbiota community and antibiotic resistance genes in the soil and earthworm gut
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Are earthworms the victim, facilitator or antidote of antibiotics and antibiotic resistance at the soil-animal-human interface? A One-Health perspective
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.176829openalex-snapshot
Promotion of antibiotic-resistant genes dissemination by the micro/nanoplastics in the gut of snail Achatina fulica
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Garden fruit chafer (Pachnoda sinuata L.) accelerates recycling and bioremediation of animal waste
inferred← citeshttps://doi.org/10.1016/j.watres.2025.124803openalex-snapshot
Swine farming emissions drive deterministic assembly of antibiotic resistance genes in receiving River: A new ecological perspective
inferred← citeshttps://doi.org/10.1021/acs.est.0c03893openalex-snapshot
Fates of Antibiotic Resistance Genes in the Gut Microbiome from Different Soil Fauna under Long-Term Fertilization
inferred← citeshttps://doi.org/10.1021/acs.est.0c04849openalex-snapshot
Long-Term Fertilization History Alters Effects of Microplastics on Soil Properties, Microbial Communities, and Functions in Diverse Farmland Ecosystem
inferred← citeshttps://doi.org/10.1021/acs.est.0c08752openalex-snapshot
Insights into the Role of the Fungal Community in Variations of the Antibiotic Resistome in the Soil Collembolan Gut Microbiome
inferred← citeshttps://doi.org/10.1021/acs.est.1c00811openalex-snapshot
Deciphering Potential Roles of Earthworms in Mitigation of Antibiotic Resistance in the Soils from Diverse Ecosystems
inferred← citeshttps://doi.org/10.1021/acs.est.1c08733openalex-snapshot
Does Plant Identity Affect the Dispersal of Resistomes Above and Below Ground?
inferred← citeshttps://doi.org/10.1021/acs.est.3c06513openalex-snapshot
Effects of Zinc Thiazole and Oxytetracycline on the Microbial Metabolism, Antibiotic Resistance, and Virulence Factor Genes of Soil, Earthworm Gut, and Phyllosphere
inferred← citeshttps://doi.org/10.1021/acs.est.4c05829openalex-snapshot
Antibiotics and Pesticides Enhancing the Transfer of Resistomes among Soil-Bayberry-Fruit Fly Food Chain in the Orchard Ecosystem
inferred← citeshttps://doi.org/10.1021/acs.est.5c15257openalex-snapshot
Microplastics in Motion: How Earthworm Guts Become Microbial Gateways through Plastic Surface Dynamics
inferred← citeshttps://doi.org/10.1021/acsenvironau.2c00056openalex-snapshot
Hormetic Effect of Pyroligneous Acids on Conjugative Transfer of Plasmid-mediated Multi-antibiotic Resistance Genes within Bacterial Genus
inferred← citeshttps://doi.org/10.1038/s41396-021-01103-9openalex-snapshot
Soil plastispheres as hotspots of antibiotic resistance genes and potential pathogens
inferred← citeshttps://doi.org/10.1080/09593330.2025.2585215openalex-snapshot
Earthworm gut as an enabler for the dissemination of tetracycline resistance genes: evidence from controlled feeding experiments
inferred← citeshttps://doi.org/10.1101/2022.01.04.474879openalex-snapshot
Core Microbiota Drive the Prevalence of Extracellular Antibiotic Resistome in the Water Compartments
inferred← citeshttps://doi.org/10.1186/s40168-021-01144-4openalex-snapshot
Trophic level drives the host microbiome of soil invertebrates at a continental scale
inferred← citeshttps://doi.org/10.20944/preprints202403.0001.v1openalex-snapshot
High-throughput Analysis of Department-Specific Dynamic Patterns of Bacterial Communities and Antibiotic Resistance in the Hospital Indoor Environments
inferred← citeshttps://doi.org/10.3389/fmicb.2022.916875openalex-snapshot
Changes in the Abundance and Community Complexity of Soil Nematodes in Two Rice Cultivars Under Elevated Ozone
inferred← citeshttps://doi.org/10.3390/antibiotics12091471openalex-snapshot
Overview of Direct and Indirect Effects of Antibiotics on Terrestrial Organisms
inferred← citeshttps://doi.org/10.3390/soilsystems7020055openalex-snapshot
Assessment of the Impact of Ceftriaxone on the Functional Profile of Soil Microbiota Using Biolog EcoPlateTM
inferred← citeshttps://doi.org/10.6084/m9.figshare.16650170openalex-snapshot
Additional file 2 of Trophic level drives the host microbiome of soil invertebrates at a continental scale
inferred← citeshttps://doi.org/10.6084/m9.figshare.16650176openalex-snapshot
Additional file 3 of Trophic level drives the host microbiome of soil invertebrates at a continental scale
inferred← citeshttps://doi.org/10.6084/m9.figshare.16650182openalex-snapshot
Additional file 4 of Trophic level drives the host microbiome of soil invertebrates at a continental scale
inferred← citeshttps://doi.org/10.6084/m9.figshare.16650188openalex-snapshot
Additional file 5 of Trophic level drives the host microbiome of soil invertebrates at a continental scale
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