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47 results for “Phytotoxicity”
Nanoplastic_soybean_phytotoxicity_48 hours
<p>The data obtained in frame of research concerning the influence of nanoplastic particles (polystyrene) on soybean seeds and seedlings.</p> <p>The nanoplastic was applied at two concentrations - 10 and 100 mg/l, for 48 hours. </p> <p>The data include:</p> <ul> <li>germination rate</li> <li>growth (roots length)</li> <li>cytotoxicity: cell viability assessed by Evans Blue assay</li> <li>oxidative status: reduced and oxidized glutathione levels (GSH and GSSG)</li> <li>lipid peroxidation: TBARS levels</li> </ul>
Fig. 5 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 5. Phytotoxic effects of different metabolites on seed germination and seedling growth of S. viridis in Petri dishes of experiment: (a) control; (b) 1; (c) 2; (d) 3; (e) 4; (f) 8.
Fig. 5 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 5. Regression analysis of experimental versus calculated 13C NMR chemical shifts of 1a and 2a, linear fitting is shown as a line.
Fig. 7 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 7. Phytotoxic effects of compound 2, 20, 21, 22, 25, 27, and glyphosate (positive control) on the growth of the roots and shoots of L. sativa seedlings at concentrations of 200, 100, 50, 25 μg/mL, respectively. (A) L. sativa shoot, (B) L. sativa root. (*) p <0.05, (**) p <0.01, and (***) p <0.001 versus the control group.
Fig. 6 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 6. Phytotoxic effects of compound 2, 3, 15, 18, 20, 25, 29, 32, and glyphosate (positive control) on the growth of the roots and shoots of L. perenne seedlings at concentrations of 200, 100, 50, 25 μg/mL, respectively. (A) L. perenne root, (B) L. perenne shoot. (*) p <0.05, (**) p <0.01, and (***) p <0.001 versus the control group.
Fig. 5 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 5. Phytotoxic effects of the MeOH extract, the EtOAc fraction, and the n-BuOH fraction on the growth of the roots and shoots of L. perenne and L. sativa seedlings at concentrations of 400, 200, 100, 50 μg/mL, respectively. (A) L. perenne root, (B) L. perenne shoot, (C) L. sativa root, (D) L. sativa shoot. (*) p <0.05, (**) p <0.01, and (***) p <0.001 versus the control group.
QTL mapping and marker development for tolerance to sulfur phytotoxicity in melon (Cucumis Melo)
Open the record for dataset details and reuse information.
Fig. 4 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 4. Experimental and calculated ECD spectra of 1–4 and 8.
Fig. 7 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 7. Symptoms of 1–4 and 8 against the weed seeding growth of S. viridis.
Fig. 3 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 3. Key NOE correlations of 1–5 and 8.
Fig. 6 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 6. Effect of different specialized metabolites on seed germination of S. viridis.
Fig. 1 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 1. Chemical structures of 1–8.
Fig. 2. Key 1H–1H in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 2. Key 1H–1H COSY, and HMBC correlations of 1–5 and 8.
Fig. 3. ROESY and 1D in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 3. ROESY and 1D NOE correlations of 1a and 2a.
Fig. 2 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 2. COSY and key HMBC correlations of 1 and 2.
Fig. 1 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 1. Chemical Structures of 1, 2, and previously reported 3-decalinoyltetramic acid derivatives.
Fig. 7 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 7. Phytotoxicity toward roots and hypocotyls growth of A. retroflexus L. and A. hybrid.
Fig. 4 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 4. Comparison between calculated and experimental ECD spectra of compounds 1 and 2.
Fig. 3 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 3. ORTEP drawing of 1, 3, and 27.
Fig. 4 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 4. (a) HMBC and 1H–1H COSY (b) NOESY correlations of compound 25.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.