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1,071 results for “shield”

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zenodo28/100

FIGURE 6 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 6. Abdominal ventrites of Radicitus spp. A) R. ayacucho, B) R. granitum.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 3 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 3. Heads of Radicitus spp., ventral view. A) R. ayacucho, B) R. granitum.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 1 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 1. Radicitus ayacucho, dorsal, ventral, and lateral habitus (paratype).

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 5 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 5. Details of Radicitus granitum. A) thoracic sternum. B) metafemur.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 8 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 8. Distribution of Radicitus spp.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 2 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 2. Radicitus granitum, dorsal, ventral, and lateral habitus (paratype).

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 4 in A new genus of egg case-carrying water scavenger beetle from the Guiana Shield (Coleoptera: Hydrophilidae: Acidocerinae)

FIGURE 4. Elytra of Radicitus spp. A) R. ayacucho, B) R. granitum.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 8 in Gynacantha dryadula sp. nov. from the Guiana Shield (Odonata, Anisoptera: Aeshnidae)

FIGURE 8. Larval habitat of Gynacantha dryadula sp. nov., at type locality, in Brazil.

opennotspecifiedDec 2017View details →
zenodo28/100

FIGURE 9 in Gynacantha dryadula sp. nov. from the Guiana Shield (Odonata, Anisoptera: Aeshnidae)

FIGURE 9. Distribution of Gynacantha dryadula sp. nov. in the Guiana Shield (type locality red).

opennotspecifiedDec 2017View details →
zenodo28/100

Supplementary Material: molecular geometries and isotropic NMR shieldings of the systems used to test CD-CASSCF and CD-GIAO-CASSCF

Open the record for dataset details and reuse information.

opencc-by-4.0Oct 2023View details →
zenodo28/100

FIGURE 13. Living Eulithoxenus emeljanovi. A, B, E in Ptosoproctus gen. nov., a new genus with two new species of Shield-back Katydid with the first record of genus Eulithoxenus Bey-Bienko, 1951 from China (Orthoptera: Tettigoniidae: Tettigoniinae: Drymadusini)

FIGURE 13. Living Eulithoxenus emeljanovi. A, B, E. male; C, D, F. female.

opennotspecifiedNov 2021View details →
zenodo28/100

Data for Model test on the passive failure of slurry shield tunneling in circular-gravel stratum

<p>Data for Model test on the passive failure of slurry shield tunneling in circular-gravel stratum.</p>

opencc-by-4.0Dec 2021View details →
zenodo28/100

FIGURE 15 in New species and new distributional records of the hygropetric water scavenger beetle genus Oocyclus Sharp (Coleoptera, Hydrophilidae) from the Brazilian Shield

FIGURE 15. Distribution map for species of Oocyclus previously known in Brazil.

opennotspecifiedJan 2022View details →
zenodo28/100

FIGURE 14 in New species and new distributional records of the hygropetric water scavenger beetle genus Oocyclus Sharp (Coleoptera, Hydrophilidae) from the Brazilian Shield

FIGURE 14. Distribution map for new Oocyclus species in Brazil.

opennotspecifiedJan 2022View details →
dryad28/100

Removal of gut symbiotic bacteria negatively affects life history traits of the shield bug, Graphosoma lineatum

<p><span>Bacterial Symbionts play an important biological role in their host. <i>G. lineatum</i> harbor bacterial symbiont in the enclosed crypts of the midgut. It seems that the bacterial symbiont play important role in the insect. Therefore, in this study, the role of bacterial symbiont in the shield bug, <i>Graphosoma lineatum</i> (Heteroptera, Pentatomidae) was investigated. To do this symbiont elimination was performed using surface sterilization of the eggs. Then, we utilized <span>age-stage, two-sex life table analysis</span> to confirm the biological importance of bacterial symbiont in <i>G. lineatum</i>. According to our results symbiont removal had a significantly negative effect on the biology of the insect. These results clearly indicate this symbiont is essential for normal growth and reproduction.</span></p>

opencc-zeroApr 2022View details →
zenodo28/100

Distribution. Known only from Guyana and Suriname in the Guiana Shield. in Phyllostomidae

Distribution. Known only from Guyana and Suriname in the Guiana Shield.

opennotspecifiedOct 2019View details →
zenodo28/100

Distribution. Known only from Guiana Shield in Guaviare and Vaupés depart ments, E Colombia. in Phyllostomidae

Distribution. Known only from Guiana Shield in Guaviare and Vaupés depart ments, E Colombia.

opennotspecifiedOct 2019View details →
zenodo28/100

Distribution. Guiana Shield tepuis in S Venezuela and adjacent areas of Guyana and N Brazil. in Cricetidae

Distribution. Guiana Shield tepuis in S Venezuela and adjacent areas of Guyana and N Brazil.

opennotspecifiedNov 2017View details →
zenodo28/100

Toxin-producing endosymbionts shield pathogenic fungus against micropredators: Supplementary Information Videos

<p><strong>ABSTRACT</strong></p> <p>The fungus <em>Rhizopus microsporus </em>harbours a bacterial endosymbiont (<em>Mycetohabitans rhizoxinica</em>) for the production of the antimitotic toxin rhizoxin. Although rhizoxin is the causative agent of rice seedling blight, the toxinogenic bacterial-fungal alliance is, however, not restricted to the plant disease. It has been detected in numerous environmental isolates from geographically distinct sites covering all five continents, thus raising the question on the ecological role of rhizoxin beyond rice seedling blight.</p> <p>Here we show that rhizoxin serves the fungal host in fending off protozoan and metazoan predators. Fluorescence microscopy and co-culture experiments with the fungivorous amoeba <em>Protostelium aurantium</em> revealed that ingestion of <em>R. microsporus</em> spores is toxic to <em>P. aurantium</em>. This amoebicidal effect is caused by the dominant bacterial rhizoxin congener rhizoxin S2, which is also lethal towards the model nematode <em>Caenorhabditis elegans</em>. By combining stereomicroscopy, automated image analyses, and quantification of nematode movement we show that the fungivorous nematode <em>Aphelenchus avenae </em>actively feeds on <em>R. microsporus</em> that is lacking endosymbionts, while worms co-incubated with symbiotic <em>R. microsporus </em>are significantly less lively.</p> <p>This work uncovers an unexpected ecological role of rhizoxin as shield against micropredators. This finding suggests that predators may function as an evolutionary driving force to maintain toxin-producing endosymbionts in non-pathogenic fungi.</p> <p>&nbsp;</p> <p><strong>Legends for the Supplementary Information Videos</strong></p> <p><strong>Video S1</strong>. Predation of <em>Protostelium aurantium</em> on swollen spores from <em>Rhizopus microsporus</em>. Timelapse<br> movie showing ingestion of a swollen <em>R. microsporus</em> spore (stained with FITC) by <em>P. aurantium</em>. Scale<br> bar: 5 &mu;m.</p> <p><strong>Video S2.</strong> <em>Aphelenchus avenae</em> co-incubated with symbiotic<em> Rhizopus microsporus. R. microsporus</em><br> ATCC62417 was co-incubated with <em>A. avenae </em>for 24 hrs in a micro-channel slide (Ibidi). Time-lapse movie,<br> recorded on a spinning disc microscope, showing dead/unhealthy nematodes. Scale bar: 100 &mu;m.</p> <p><strong>Video S3.</strong> <em>Aphelenchus avenae</em> movement after incubation with solvent control (DMSO). Time-lapse<br> movie, recorded on a spinning disc microscope, showing healthy nematodes. Scale bar: 200 &mu;m.</p> <p><strong>Video S4.</strong> <em>Aphelenchus avenae</em> movement after incubation with 100 &mu;M rhizoxin S2. Time-lapse<br> movie, recorded on a spinning disc microscope, showing unhealthy nematodes. Scale bar: 200 &mu;m.</p> <p><strong>Video S5. </strong><em>Aphelenchus avenae</em> movement after incubation with 250 &mu;M rhizoxin S2. Time-lapse<br> movie, recorded on a spinning disc microscope, showing dead/unhealthy nematodes. Scale bar: 200 &mu;m.</p> <p><strong>Video S6. </strong><em>Aphelenchus avenae</em> movement after incubation with 500 &mu;M rhizoxin S2. Time-lapse<br> movie, recorded on a spinning disc microscope, showing dead/unhealthy nematodes. Scale bar: 200 &mu;m.</p> <p><strong>Video S7</strong>. <em>Aphelenchus avenae</em> movement after incubation with 114 &mu;M ivermectin (positive<br> control). Time-lapse movie, recorded on a spinning disc microscope, showing dead/unhealthy<br> nematodes. Scale bar: 200 &mu;m.</p> <p><strong>Video S8.</strong> Segmented worms and their summarized tracks. The segmented worms are shown in white,<br> whereas the worm outlines at each time point are shown in yellow. The time series shows the individual<br> worms per time point, whereas the yellow outlines are superimposed over the entire time series and shown<br> at each time point of the video.</p> <p><strong>Video S9.</strong> The segmented worms and their tracks of a time series experiment. The worms and the<br> tracks are shown here as provided by the automated tracking algorithm applied to a time series experiment.<br> The worms are coloured randomly, whereas the tracks (thin lines) are coloured from blue to red for each<br> track, blue corresponding to time zero and red to the final time point. When worms merge, they become of<br> the same colour until they separate again.</p> <p><strong>Video S10.</strong> The X component of the per-worm and per time-point velocity vector of each worm as a<br> function of the Y component of the velocity vector. The time series shows the velocity vector<br> components at individual time points, playing from time zero to the final time point. Line colours correspond<br> to the time, whereas the worm colours indicate the area of the worm, see colour scale bars at the bottom of<br> the window.</p> <p><strong>Video S11</strong>. A segmented worm and its footprint for LR = 11.5. The orange objects shows the segmented<br> worm at each time point per movie frame, whereas the red area shows the worm&#39;s footprint calculated for<br> the entire time series.<br> 14</p> <p><strong>Video S12</strong>. A segmented worm and its footprint for LR = 4.0. The green object corresponds to the<br> segmented worm shown at each time point, the orange area indicates the footprint of this worm, calculated<br> for the entire time series.</p>

opencc-by-4.0Jul 2022View details →
zenodo28/100

Viking Shield Practice

6 hours 4K Textures Aimed to get as low poly as possible Source: Objaverse 1.0 / Sketchfab

opencc-by-nc-1.0Oct 2021View details →

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Allen Brain Atlas

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
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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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

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Last verified 2026-04-29Open record

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