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51 results for “rotenone”
COI and 18S metabarcoding data from Hidden Lake (Banff National Park, Canada) over two rotenone applications between 2018 and 2020.
Water samples were taken in Hidden Lake at five different time points around two rotenone applications: (i) five weeks prior to the first rotenone application, on July 12 2018; (ii) approximately three weeks after the first application of rotenone, on 7 September 2018; (iii) approximately 10 months after the first rotenone application, on 10 July 2019; (iv) four weeks following the final treatment of rotenone on the 17 September 2019; and (v) one year after the final rotenone treatment, on 19 August 2020. For each time point there is a pelagic, a littoral and a profundal sample. COI and 18S metabarcoding methods were used to produce community data. The objective of this study was to assess the non-target effect of rotenone application (in summer 2018 and 2019) on aquatic communities (i.e. phytoplankton, fungi, zooplankton and benthic macroinvertebrates).
Brook trout (Salvelinus fontinalis) cyt b qPCR data from Hidden Lake (Banff National Park, Canada) over two rotenone applications between 2018 and 2020.
Water samples were taken in Hidden Lake at five different time points around two rotenone applications: (i) five weeks prior to the first rotenone application, on July 12 2018; (ii) approximately three weeks after the first application of rotenone, on 7 September 2018; (iii) approximately 10 months after the first rotenone application, on 10 July 2019; and (iv) one year after the final rotenone treatment, on 19 August 2020. For each time point, four pelagic and four littoral water samples were taken from Hidden Lake, as well as 8 to 13 water samples from Hidden Creek and Coral Creek for a total of 16 to 21 samples per time point. Quantitative PCR (qPCR) method was used to produce brook trout (Salvelinus fontinalis) cytochrome b copy number for each sample. The objective of this study was use eDNA to assess the efficacy of invasive brook trout removal using rotenone.
Fig. 6 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 6. The concentration of rotenone in brain tissue afer treatment.* indicates significant difference between the 2 treatments at the same point in time (P <0.05, Tukey honest significant difference tests).
Fig. 4 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 4. The concentration of rotenone in hemolymph afer treatment.* indicates significant difference between the 2 treatments at the same point in time (P <0.05, Tukey honest significant difference tests).
Fig. 3 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 3. The concentration of rotenone in midgut tissue afer treatment.* indicates significant difference between the 2 treatments at the same point in time (P <0.05, Tukey honest significant difference tests).
Fig. 1 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 1. Liquid chromatogram (A: rotenone standard, B: excreta, C: hemolymph, D: brain, E: ventral nerve cord, F: midgut).
Fig. 2 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 2. The concentration of rotenone in excreta afer treatment.* indicates significant difference between the 2 treatments at the same point in time (P <0.05, Tukey honest significant difference tests).
Fig. 7 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 7. Cells of Spodoptera litura midgut peritrophic membrane (A: control, B: rotenone, C: rotenone + cinnamon oil). The arrows show the change in cell structure in response to treatment. Note that in A the cells are single, packed, and clearly visible, whereas in B the cell spacing is wider, and in C there is slightly wider cell spacing, and abnormality of the membrane.
Fig. 5 in Addition of cinnamon oil improves toxicity of rotenone to Spodoptera litura (Lepidoptera: Noctuidae) larvae
Fig. 5. The concentration of rotenone in ventral nerve cord tissue afer treatment.* indicates significant difference between the 2 treatments at the same point in time (P <0.05, Tukey honest significant difference tests).
Mechanism of rotenone binding to respiratory complex I depends on ligand flexibility
<p>Snapshots from MD simulations (with umbrella sampling and metadynamics) of<br> respiratory complex I. Only subunits ND1, NDUFS2 and NDUFS7 (with the membrane spanning N-terminus<br> truncated) and rotenone are shown in binding mode (see Fig. 2 of main paper): </p> <p>1) ROT1: configurations/rot1.pdb<br> 2) pre-redox: configurations/rot1.5.pdb<br> 3) ROT2: configurations/rot2.pdb</p> <p>Force-field and topology files in GROMACS format:</p> <p>4) Bonded parameters: parameters/rotenoids_ffBonded.itp<br> 5) Rotenone: parameters/rot.itp<br> 6) Dehydrated derivative: parameters/dehyd_rot.itp</p>
Datatset of exposure of rotenone and moringa oleifera on larvae of zebra fish
<p>This dataset contains:</p> <p>1. List of tools and utensils used</p> <p>2. Observation result of moringa oleifera</p> <p>3. Observation result of length of zebra fish after exposure </p>
dataset for paper entitled "Effect of Moringa Oleifera Leaf Extract On Body Length, Malondialadehyd and Interleukin-6 Levels in Zebrafish Larvae (Danio Rerio) Induced Stunting Model with Rotenone"
<p>The dataset consist of:</p> <p>1. Appendices of tools and material used for laboratory research</p> <p>2. Certificate of ethical test </p> <p>3. Data of moringa oleifera controls</p> <p>4. Data of zebrafish growth </p>
Unique nigral and cortical pathways implicated by epigenomic and transcriptional analyses in a rotenone rat model of Parkinson’s disease [ChIP-Seq]
GEO Series GSE280519. Rattus norvegicus. 38 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Acute and delayed transcriptomics changes in 3D LUHMES exposed to rotenone
GEO Series GSE116280. Homo sapiens. 24 samples. Type: Expression profiling by array.
Dynamics in zebrafish development define transcriptomic specificity after angiogenesis inhibitor exposure (Sorafenib and Rotenone)
GEO Series GSE270785. Danio rerio. 57 samples. Type: Expression profiling by high throughput sequencing.
Global gene profiling of rotenone-induced neuronal death
GEO Series GSE22997. Mus musculus. 13 samples. Type: Expression profiling by array.
The conserved DNMT1-dependent methylation regions in human cells are vulnerable to to neurotoxicant rotenone exposure
GEO Series GSE147617. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
RNA-seq of the killifish N.furzeri during normal aging (cross-sectional and longitudinal study) and treatment with rotenone
GEO Series GSE66712. Nothobranchius furzeri. 185 samples. Type: Expression profiling by high throughput sequencing.
RNA-seq of human fibroblasts during normal aging and during aging with rotenone perturbation
GEO Series GSE64553. Homo sapiens. 60 samples. Type: Expression profiling by high throughput sequencing.
Deep sequencing of endogenous mRNA from Caenorhabditis elegans in the presence and absence of rotenone at 4 different time points
GEO Series GSE46051. Caenorhabditis elegans. 22 samples. Type: Expression profiling by high throughput sequencing.
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