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Environmentally Relevant Concentrations of the Flame Retardant Tris(1,3-dichloro-2-propyl) Phosphate Inhibit the Growth and Reproduction of Earthworms in Soil

https://doi.org/10.1021/acs.estlett.9b00227
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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/s00128-016-1898-0openalex-snapshot
A Review of Organophosphate Esters in the Environment from Biological Effects to Distribution and Fate
inferredcites →https://doi.org/10.1007/s00244-014-0125-4openalex-snapshot
Growth Inhibition and Altered Gene Transcript Levels in Earthworms (Eisenia fetida) Exposed to 2,2′,4,4′-Tetrabromodiphenyl Ether
inferredcites →https://doi.org/10.1007/s11356-018-3156-yopenalex-snapshot
Levels, distribution, and sources of organophosphate flame retardants and plasticizers in urban soils of Shenyang, China
inferredcites →https://doi.org/10.1016/j.aquatox.2014.11.001openalex-snapshot
Bioconcentration, metabolism and neurotoxicity of the organophorous flame retardant 1,3-dichloro 2-propyl phosphate (TDCPP) to zebrafish
inferredcites →https://doi.org/10.1016/j.chemosphere.2012.03.067openalex-snapshot
Phosphorus flame retardants: Properties, production, environmental occurrence, toxicity and analysis
inferredcites →https://doi.org/10.1016/j.chemosphere.2017.09.112openalex-snapshot
Organophosphate ester flame retardants in Nepalese soil: Spatial distribution, source apportionment and air-soil exchange assessment
inferredcites →https://doi.org/10.1016/j.chemosphere.2018.08.083openalex-snapshot
Environmentally relevant concentrations of the flame retardant tris(1,3-dichloro-2-propyl) phosphate change morphology of female zebrafish
inferredcites →https://doi.org/10.1016/j.ecoenv.2011.09.009openalex-snapshot
Effects of 1,2,4-trichlorobenzene on the enzyme activities and ultrastructure of earthworm Eisenia fetida
inferredcites →https://doi.org/10.1016/j.ejsobi.2011.11.005openalex-snapshot
Effects of fluoranthene on the growth, bioavailability and anti-oxidant system of Eisenia fetida during the ageing process
inferredcites →https://doi.org/10.1016/j.envpol.2006.11.030openalex-snapshot
Differences in p,p′-DDE bioaccumulation from compost and soil by the plants Cucurbita pepo and Cucurbita maxima and the earthworms Eisenia fetida and Lumbricus terrestris
inferredcites →https://doi.org/10.1016/j.envpol.2013.12.012openalex-snapshot
Species-dependent effects of biochar amendment on bioaccumulation of atrazine in earthworms
inferredcites →https://doi.org/10.1016/j.envpol.2016.09.039openalex-snapshot
Parental transfer of tris(1,3-dichloro-2-propyl) phosphate and transgenerational inhibition of growth of zebrafish exposed to environmentally relevant concentrations
inferredcites →https://doi.org/10.1016/j.envpol.2017.04.090openalex-snapshot
Fate and O-methylating detoxification of Tetrabromobisphenol A (TBBPA) in two earthworms (Metaphire guillelmi and Eisenia fetida)
inferredcites →https://doi.org/10.1016/j.envpol.2017.06.024openalex-snapshot
Time-dependent inhibitory effects of Tris(1, 3-dichloro-2-propyl) phosphate on growth and transcription of genes involved in the GH/IGF axis, but not the HPT axis, in female zebrafish
inferredcites →https://doi.org/10.1016/j.envpol.2017.06.062openalex-snapshot
Metabolomics analysis of TiO 2 nanoparticles induced toxicological effects on rice ( Oryza sativa L.)
inferredcites →https://doi.org/10.1016/j.envpol.2017.11.098openalex-snapshot
Metabolism of tri-n-butyl phosphate in earthworm Perionyx excavatus
inferredcites →https://doi.org/10.1016/j.scitotenv.2018.01.013openalex-snapshot
Occurrence and distribution of organophosphate flame retardants (OPFRs) in soil and outdoor settled dust from a multi-waste recycling area in China
inferredcites →https://doi.org/10.1016/s0014-5793(03)00437-xopenalex-snapshot
Phosphoinositide signaling disorders in human diseases
inferredcites →https://doi.org/10.1021/acs.est.5b03294openalex-snapshot
Effects of Tris(1,3-dichloro-2-propyl) Phosphate on Growth, Reproduction, and Gene Transcription of Daphnia magna at Environmentally Relevant Concentrations
inferredcites →https://doi.org/10.1021/acs.est.5b03849openalex-snapshot
Environmentally Relevant Concentrations of the Flame Retardant Tris(1,3-dichloro-2-propyl) Phosphate Inhibit Growth of Female Zebrafish and Decrease Fecundity
inferredcites →https://doi.org/10.1021/acs.est.6b05484openalex-snapshot
Organophosphate Esters in Sediment of the Great Lakes
inferredcites →https://doi.org/10.1021/acs.est.7b04569openalex-snapshot
Whole-Life-Stage Characterization in the Basic Biology of Daphnia magna and Effects of TDCIPP on Growth, Reproduction, Survival, and Transcription of Genes
inferredcites →https://doi.org/10.1021/acs.est.8b03730openalex-snapshot
Tris(1,3-dichloro-2-propyl) Phosphate Exposure During the Early-Blastula Stage Alters the Normal Trajectory of Zebrafish Embryogenesis
inferredcites →https://doi.org/10.1021/es061893jopenalex-snapshot
Surfactants Differentially Impact p,p ‘-DDE Accumulation by Plant and Earthworm Species
inferredcites →https://doi.org/10.1021/es401265qopenalex-snapshot
Toxicogenomic Responses of Zebrafish Embryos/Larvae to Tris(1,3-dichloro-2-propyl) Phosphate (TDCPP) Reveal Possible Molecular Mechanisms of Developmental Toxicity
inferredcites →https://doi.org/10.1021/es9800941openalex-snapshot
Evaluation of Spiking Procedures for the Introduction of Poorly Water Soluble Contaminants into Soil
inferredcites →https://doi.org/10.1038/nrrheum.2014.2openalex-snapshot
The skeletal muscle arachidonic acid cascade in health and inflammatory disease
inferredcites →https://doi.org/10.1038/s41598-018-34814-9openalex-snapshot
Untargeted metabolomics reveals transformation pathways and metabolic response of the earthworm Perionyx excavatus after exposure to triphenyl phosphate
inferredcites →https://doi.org/10.1039/c8en00703aopenalex-snapshot
Cellular response of Chlorella pyrenoidosa to oxidized multi-walled carbon nanotubes
inferredcites →https://doi.org/10.1080/10643389.2011.574100openalex-snapshot
Evaluation of Exposure Metrics for Effect Assessment of Soil Invertebrates
inferredcites →https://doi.org/10.1097/00041433-200206000-00007openalex-snapshot
Cytochrome P450 pathways of arachidonic acid metabolism
inferredcites →https://doi.org/10.1210/en.2008-1338openalex-snapshot
Hormone-Activated Estrogen Receptors in Annelid Invertebrates: Implications for Evolution and Endocrine Disruption
inferredcites →https://doi.org/10.1289/ehp.1205316openalex-snapshot
Early Zebrafish Embryogenesis Is Susceptible to Developmental TDCPP Exposure

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1007/978-3-031-64510-5_19openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10311-022-01507-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11368-022-03146-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s42832-021-0084-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44169-025-00103-6openalex-snapshot
Tris (1, 3-dichloro-2-Propyl) Phosphate (TDCIPP) in the Environment and its Potential Effects on Human Health
inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106401openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.131684openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111462openalex-snapshot
Synergistic growth inhibition effect of TiO2 nanoparticles and tris(1,3-dichloro-2-propyl) phosphate on earthworms in soil
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113798openalex-snapshot
Environmentally relevant concentrations of tris (1,3-dichloro-2-propyl) phosphate induce growth inhibition and oxidative stress in silver carp (Hypophthalmichthys molitrix) larvae
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118724openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envint.2024.108496openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114376openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2021.117965openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2022.119120openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120785openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120862openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eti.2022.102988openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jece.2025.115340openalex-snapshot
Environmental safety perspectives on organophosphate flame retardants: Current strategies and advancements in their environmental removal and detection
inferred← citeshttps://doi.org/10.1016/j.jes.2022.07.032openalex-snapshot
Chlorine substitution-dependent toxicities of polychlorinated biphenyls to the earthworm Eisenia fetida in soil
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.122850openalex-snapshot
Tri-n-butyl phosphate induced earthworm intestinal damage by influencing nutrient absorption and energy homeostasis of intestinal epithelial cells
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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.2023.131161openalex-snapshot
A critical review on sources and environmental behavior of organophosphorus flame retardants in the soil: Current knowledge and future perspectives
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131303openalex-snapshot
Earthworms enhance the bioremediation of tris(2-butoxyethyl) phosphate-contaminated soil by releasing degrading microbes
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.132095openalex-snapshot
Established and emerging organophosphate esters (OPEs) and the expansion of an environmental contamination issue: A review and future directions
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133567openalex-snapshot
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Congener-specific fate and impact of microcystins in the soil-earthworm system
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135351openalex-snapshot
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