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A Survey of Antimicrobial Biocides in Direct-to-Consumer Products in Australia
<p>Antimicrobial biocides such as disinfectants and preservatives are extremely widely used to control microbial growth, but are not regulated like antibiotics. Unfortunately, there is increasing evidence that many biocides can compromise antibiotic efficacy. The aim of this survey was to determine which biocides are most commonly found in products available to the public in Australia. Over 350 non-redundant products were surveyed and the results collated and presented by product category and biocide class. This data is a startpoint to understand overall biocide usage in Australia. Results and survey background are provided in the pdf report, and the full data on products surveyed and biocides present is available as a spreadsheet.</p>
Bacteroides cellulosilyticus-directed glycans relieve colitis
<p>Bacteroides cellulosilyticus correlates with inflammatory bowel disease (IBD). Targeting an increase in abundance of B. cellulosilyticus is a feasible approach to treating IBD. Although B. cellulosilyticus is responsive to dietary components, untargeted manipulation cannot focus on target microbe and can lead to an increase in harmful bacteria in the microbiota. Despite breakthroughs in methods for regulating specific microbes, the protocols are expensive, time-consuming, and difficult to follow. Glycans based on microbial-carbohydrate-active enzymes (CAZymes) that target a specific microbiota would provide a potential solution.</p>
Printed Dual-Frequency Directional Antenna Loaded with Dual-Parasitic Strip
<p>Dataset 1-23 are the raw data from CST studio suite analysis software (CST). A series of simulations are performed on the MS-to-CPS transition, the dual dipole element, the reflectors, and the parasitic strip to determine the optimal antenna design. Dataset 24-28 are the raw data from the measured results whose are compared with the simulated results of the optimal antenna design.</p> <p><strong>Additional Supporting Information</strong></p> <p>Dataset 1 and 2 are the raw data of Figure 2.</p> <p>Dataset 3 is the raw data of Figure 3.</p> <p>Dataset 4, 5, and 6 are the raw data of Figure 5.</p> <p>Dataset 7 is the raw data of Figure 6.</p> <p>Dataset 8 is the raw data of Figure 9.</p> <p>Dataset 9 is the raw data of Figure 10.</p> <p>Dataset 10 is the raw data of Figure 11.</p> <p>Dataset 11 and 12 are the raw data of Figure 12.</p> <p>Dataset 13 and 14 are the raw data of Figure 13.</p> <p>Dataset 15 and 16 are the raw data of Figure 14.</p> <p>Dataset 17 and 18 are the raw data of Figure 15.</p> <p>Dataset 19 and 20 are the raw data of Figure 16.</p> <p>Dataset 21 is the raw data of Figure 17.</p> <p>Dataset 22 is the raw data of Figure 18.</p> <p>Dataset 23 is the raw data of Figure 19.</p> <p>Dataset 24 is the raw data of Figure 21.</p> <p>Dataset 25, 26, 27, and 28 are the raw data of Figure 22.</p>
Direct visualization of electronic transport in a quantum anomalous Hall insulator
<p>Source data for "Direct visualization of electronic transport in a quantum anomalous Hall insulator"</p>
Localization files for "Imaging proteins sensitive to direct fusions using transient peptide-peptide interactions"
<p>Localization csv files for super-resolution images taken and analysed for "Imaging proteins sensitive to direct fusions using transient peptide-peptide interactions". Single localizations were processed using the Peak Fit function of the Fiji (Java 8 2017 release) GDSC SMLM plugin, using a signal strength threshold of 30, a minimum photon threshold of 100, and a precision threshold of 15-30 nm (precision threshold used is indicated in the file name). </p>
Figure 16 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 16. Scanning electron micrographs of the secretion. A, distal end of the infudibuliform complex with the extruded filaments. B, C, detail of filaments showing the granular surface.
Figure 15 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 15. Scanning electron micrographs of the cerci of Recent projapygids (genera indet.) expelling the glandular substance. A–C, different magnifications of cerci of a specimen from Brazil showing the solidified secretion forming filamentous masses. D, distal part of cerci of a Costa Rican specimen showing an incipient secretion. Arrows indicate the glandular substance in C and D. In A, the box labelled B corresponds to panel B; In B, the box labelled C corresponds to panel C. Abbreviations: ids, infundibuliform distal segment; ipds, infundibuliform predistal segment; ss, simple setae; tp, longitudinal tegumentary pleats. Scale bars: 1 mm in A; 0.2 mm in B; 0.05 mm in C, D.
Figure 14 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 14. Palaeoecological reconstruction of Electroprojapyx alchemicus gen. et sp. nov, using their cerci as chemical weapons for hunting a springtail in the Cretaceous amber forest. Illustration by O. Sanisidro, with scientific supervision.
Figure 8 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 8. Volume renderings of Symphylurinus sp. 1 (AMNH JZC-DR005) in Miocene Dominican amber. A, dorsal habitus. B, ventral habitus. C, right lateral habitus. All to the same scale. Scale bar: 1 mm.
Figure 7 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 7. Camera lucida drawings of Symphylurinus sp. 1 (AMNH JZC-DR005) in Miocene Dominican amber. A, left ventrolateral habitus. B, detail of right tarsi of leg III. C, right abdominal stylus V. D, right abdominal stylus VI. E, right abdominal stylus VII. F, detail of infundibuliform complex of left cercus. Abbreviations: a, apical macroseta; lp, labial palpus; M, sternal macroseta; sa, subapical macroseta; scA, lateral subcoxal appendage; stI–stVII, stylus I–VII; vm, ventromedial macroseta. C–F are to the same scale. Scale bars: 0.5 mm in A; 0.2 mm in B; 0.1 mm in C–F.
Figure 5 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 5. Volume renderings of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, dorsal habitus. B, ventral habitus. C, left lateral habitus. All to the same scale. Scale bar: 1 mm.
Figure 1 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 1. Scanning electron micrographs of Recent specimens representing the two body plans of predatory diplurans. A, Japygoidea specimen from Malta, dorsal view. B, Projapygoidea specimen from Thailand, ventral view. C, detail of cercal forceps. D, detail of right cercus. Scale bars: 2 mm in A; 0.5 mm in B.
Figure 4 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 4. Camera lucida drawings of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, detail of cerci. B, dorsal habitus. Abbreviations: lp, labial palp; scA, lateral subcoxal appendage; stI– stVII, stylus I–VII. Scale bars: 0.5 mm.
Figure 3 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 3. Photomicrographs of holotype of Symphylurinopsis punctatus gen. et sp. nov. (M-2232) in Miocene Dominican amber. A, dorsal habitus. B, detail of setigerous punctures on tergites IV–VII. C, detail of head. D, detail of cerci in ventral view. Abbreviations: gp, genital papilla; lp, labial palp; mp, maxillary palp; stVII, stylus VII. Scale bars: 0.5 mm in A; 0.1 mm in B–D.
Figure 2 in Fossil diversity in 'dawn' hexapods (Diplura: Projapygoidea), with direct evidence for being chemically predaceous in the Cretaceous
Figure 2. Holotype of Electroprojapyx alchemicus gen. et sp. nov. (AMNH JZCBu-1957) in Cretaceous Burmese amber. A, photomicrographs of left ventrolateral habitus of the dipluran fossilized in a preying-and-spraying position with its prey. B, detail of cerci with arrows pointing to the secreted substance. C, camera lucida drawing of the specimen with the secreted filaments in red. D, detail of antennae of the dipluran with the Collembola between them. Abbreviations: b, bubble; scA, lateral subcoxal appendage; stII–stVII, stylus II–VII. Scale bars: 0.5 mm in A, C, D; 0.1 mm in B.
Direct observation and measurements of subglacial deformation in a tunnel beneath Wright Lower Glacier, Antarctica
<p>Photographs and video of a tunnel excavated in the margin of Wright Lower Glacier, Antarctica</p>
Fig. 5. T in Indirect and direct acoustic aggression in cicadas: first observations in the Palaearctic genus Tibicina Amyot (Hemiptera: Cicadomorpha: Cicadidae)
Fig. 5. T. quadrisignata. (A) Waveform and spectrogram of a part of the calling signal; (B) detailed waveform correponding to the reversed window in (A); (C) waveform and spectrogram of a part of the rivalry signal; (D) detailed waveform of three successive echemes corresponding to the reversed window in (C). Features of spectrographic analysis as in figure 2.
Fig. 4. T in Indirect and direct acoustic aggression in cicadas: first observations in the Palaearctic genus Tibicina Amyot (Hemiptera: Cicadomorpha: Cicadidae)
Fig. 4. T. tomentosa. (A) Waveform and spectrogram of a part of the calling signal; (B) detailed waveform correponding to the reversed window in (A); (C) waveform and spectrogram of a part of the rivalry signal; (D) detailed waveform of seven successive echemes corresponding to the reversed window in (C). Features of spectrographic analysis as in figure 2.
Fig. 3. T in Indirect and direct acoustic aggression in cicadas: first observations in the Palaearctic genus Tibicina Amyot (Hemiptera: Cicadomorpha: Cicadidae)
Fig. 3. T. corsica fairmairei. (A) Waveform and spectrogram of a part of the calling signal; (B) detailed waveform correponding to the reversed window in (A); (C) waveform and spectrogram of a part of the rivalry signal; (D) detailed waveform of four successive echemes corresponding to the reversed window in (C). Features of spectrographic analysis as in figure 2.
Fig. 4 in Site directed mutagenesis of Catharanthus roseus (+)-vincadifformine 19-hydroxylase (CYP71BY3) results in two distinct enzymatic functions
Fig. 4. GOLD's highest rated poses for (¡)-tabersonine and (þ)-vincadifformine into the V19H model generated from the 3ruk template with and without increased flexibility in the binding site residues. ()-tabersonine (B) and (+)-vincadifformine (A) best poses are shown in a rigid binding site (top) and a flexible binding site (bottom). The 19C is labelled in both ligands (arrows), and neither ligand is docked in the correct orientation for oxidation in a rigid binding site (top. However, in a flexible binding site, (+)-vincadifformine is in the correct orientation for 19C oxidation (bottom; B), whereas ()-tabersonine is not (bottom; A). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.