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Supplementary material 1 from: Blancher P, Lefrançois E, Rimet F, Vasselon V, Argillier C, Arle J, Beja P, Boets P, Boughaba J, Chauvin C, Deacon M, Duncan W, Ejdung G, Erba S, Ferrari B, Fischer H, Hänfling B, Haldin M, Hering D, Hette-Tronquart N, Hiley A, Järvinen M, Jeannot B, Kahlert M, Kelly M, Kleinteich J, Koyuncuoğlu S, Krenek S, Langhein-Winther S, Leese F, Mann D, Marcel R, Marcheggiani S, Meissner K, Mergen P, Monnier O, Narendja F, Neu D, Onofre Pinto V, Pawlowska A, Pawlowski J, Petersen M, Poikane S, Pont D, Renevier M-S, Sandoy S, Svensson J, Trobajo R, Tünde Zagyva A, Tziortzis I, van der Hoorn B, Vasquez MI, Walsh K, Weigand A, Bouchez A (2022) A strategy for successful integration of DNA-based methods in aquatic monitoring. Metabarcoding and Metagenomics 6: e85652. https://doi.org/10.3897/mbmg.6.85652
Table S1
FIGURE 1. A, B in A multiplex PCR method for identification of two common true cutworm species (Lepidoptera: Noctuidae) tested in the central plain of Guilan province, Iran
FIGURE 1. A, B, Maize and green pepper fields damaged by true cutworm.
Figure 3 from: Nader M, El Indary S, Abi Salloum B, Abou Dagher M (2011) Combining non-invasive methods for the rapid assessment of mammalian richness in a transectquadrat survey scheme – Case Study of the Horsh Ehden Nature Reserve, North Lebanon. ZooKeys 119: 63-71. https://doi.org/10.3897/zookeys.119.1040
Figure 3 - Mammalian distribution map showing the location of mammalian activity and the location of the Motion Sensor Cameras.
Figure 3 from: Ziegler A, Seidl B (2012) Electron microscopic and preparative methods for the analysis of isopod cuticle. ZooKeys 176: 73-85. https://doi.org/10.3897/zookeys.176.2294
Figure 3 - FE-SEM micrographs of polished sagittal plane through bulk tergite samples etched at pH 6.5 A, B, C and 8.0 D, E. A Fibres in the distal exocuticle (dex) and the isle-like structure of the proximal exocuticle (pex) caused by large pore canals (pc). Fibrils or fibres (arrowheads) in the pore canals are well visible. en, endocuticle. B, C Side views of tricorn sensilla. The epicuticular unmineralised material forming the sensilla is well distinguishable from the mineralised exo- and endocuticle. ep, epicuticle; sc, epicuticular scale. D, E Mild etching reveals regions containing mineral of different solubility. Mineral within the endocuticle appears etched whereas most regions within the exocuticle (ex) remain unaltered. Note etching within pore canals of the exocuticle.
Figure 1 from: Ziegler A, Seidl B (2012) Electron microscopic and preparative methods for the analysis of isopod cuticle. ZooKeys 176: 73-85. https://doi.org/10.3897/zookeys.176.2294
Figure 1 - TEM A, G, H, I and STEM B, C, D, E, F micrographs of decalcified and EPON embedded tergites of Porcellio scaber. A Sagittal overview showing epicuticle (ep), exocuticle (ex), endocuticle (en) and membranous layer (ml), ec, epithelial cell; n, nucleus; sc, epicuticular scale. B Proximal exocuticle. Dense network of pore canals (pc) containing fibrils or fibres following the direction of the pore canal. C, D Fibres of the distal exocuticle (dex) consisting of approximately 3 nm thick unstained chitin crystallites (arrowheads) surrounded by densely stained proteins. E, F In the endocuticle single fibrils form the twisted plywood structure. The pore canals contain vertical fibrils or fibres. G, H, I Section through a cuticular thickening. The increase in cuticle thickness is brought about by an increase of the stacking height in the distal exocuticle only. H, I Details of G confirm the typical structure of fibres within the distal exocuticle.
Figure 2 from: Ziegler A, Seidl B (2012) Electron microscopic and preparative methods for the analysis of isopod cuticle. ZooKeys 176: 73-85. https://doi.org/10.3897/zookeys.176.2294
Figure 2 - STEM micrographs of non-decalcified tergites of Porcellio scaber. A Overview showing the mineralised exocuticle (ex) and endocuticle en and the unmineralised membranous layer (ml). The pore canals (arrows) are mineralised. B, C Exocuticle and epicuticle (ep). Approximately 25 nm thick fibres in the distal exocuticle (dex) and approximately 6 nm thick fibrils in the proximal exocuticle (pex). Pore canals arrows contain mineral. The inner epicuticle (iep) appears partly mineralised, and the outer epicuticle (oep) unmineralised, except epicuticular pore canals (epc). D, E Endocuticle with mineralised pore canal (arrow). Approximately 6 nm thick chitin-protein fibrils (black arrowheads) individually surrounded by mineral forming a twisted plywood structure. F, G Single mineral rods (white arrowheads) at the border between membranous layer and endocuticle.
Figure 1 from: Backwell P, Johnson L, Mantle B, Gardner J (2013) Morphometric measurements of dragonfly wings: the accuracy of pinned, scanned and detached measurement methods. ZooKeys 276: 77-84. https://doi.org/10.3897/zookeys.276.4207
Figure 1 - Estimated mean forewing lengths obtained using the four different measurement methods. Slide 1 = identifier visible; slide 2 = identifier obscured. The median, quartiles and range are shown.
Figure 1 from: Häberlein L, Cengiz P-M, Demirova I, Dwojak-Matras A, Jacobsen MW, Koterwas A, Lopez B, Metodiev T, Palianopoulou M (2019) Validation of the mapping of innovative methods and research integrity curricula. Research Ideas and Outcomes 5: e49755. https://doi.org/10.3897/rio.5.e49755
Figure 1 Visual representation of the Path2Integrity map on RI/RE curricula.
Figure 9 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 9 Chromatogram of cardiazol degraded under oxidative conditions.
Figure 3 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 3 Chemical structure of α-bromo-4-methoxyacetophenone (impurity B).
Figure 1 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 1 Chemical structure of cardiazol.
Figure 6 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 6 Chromatogram of the test solution.
Figure 2 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 2 Chemical structure of N1-Allyl-N2- (31-trifluoromethylphenylamine) thiourea (impurity A).
Figure 10 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 10 Chromatogram of cardiazol degraded under temperature conditions.
Figure 8 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 8 Chromatogram of cardiazol degraded under alkaline conditions.
Figure 5 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 5 Chromatogram of blank solution.
Figure 7 from: Drapak I, Zimenkovsky B, Ivanauskas L, Bezruk I, Perekhoda L, Muzychenko V, Logoyda L, Demchuk I (2020) HPLC method for simultaneous determination of impurities and degradation products in Cardiazol. Pharmacia 67(1): 29-37. https://doi.org/10.3897/pharmacia.67.e37004
Figure 7 Chromatogram of cardiazol degraded under acidic conditions.
Figure 3 from: Mateeva A, Peikova L, Kondeva-Burdina M, Georgieva M (2022) Development of new HPLC method for identification of metabolic degradation of N-pyrrolylhydrazide hydrazones with determined MAO- B activity in cellular cultures. Pharmacia 69(1): 15-20. https://doi.org/10.3897/pharmacia.69.e78417
Figure 3 Chromatogram demonstrating the hepatocytic metabolism of analyte at 120th min.
Figure 1 from: Mateeva A, Peikova L, Kondeva-Burdina M, Georgieva M (2022) Development of new HPLC method for identification of metabolic degradation of N-pyrrolylhydrazide hydrazones with determined MAO- B activity in cellular cultures. Pharmacia 69(1): 15-20. https://doi.org/10.3897/pharmacia.69.e78417
Figure 1 Structure of the evaluated pyrrole hydazide-hydrazone.
Scheme 1 from: Mateeva A, Peikova L, Kondeva-Burdina M, Georgieva M (2022) Development of new HPLC method for identification of metabolic degradation of N-pyrrolylhydrazide hydrazones with determined MAO- B activity in cellular cultures. Pharmacia 69(1): 15-20. https://doi.org/10.3897/pharmacia.69.e78417
Scheme 1 Hydrolysis of evaluated pyrrole hydrazide-hydrazone in different pH media.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.