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2,214 results for “Walls”
Figure 6 from: Wall-Palmer D, Hegmann M, Goetze E, Peijnenburg KTCA (2019) Resolving species boundaries in the Atlanta brunnea species group (Gastropoda, Pterotracheoidea). ZooKeys 899: 59-84. https://doi.org/10.3897/zookeys.899.38892
Figure 6 Shell apical angles of A. brunnea (Atlantic, Pacific and Indian oceans), A. vanderspoeli (Pacific Ocean) and A. turriculata (Pacific and Indian oceans) are significantly different and do not overlap.
Figure 3 from: Wall-Palmer D, Hegmann M, Goetze E, Peijnenburg KTCA (2019) Resolving species boundaries in the Atlanta brunnea species group (Gastropoda, Pterotracheoidea). ZooKeys 899: 59-84. https://doi.org/10.3897/zookeys.899.38892
Figure 3 A Distribution maps showing the collection locations for each clade identified in B. The collection location of specimens of A. turriculata forma B identified by van der Spoel (1976) from offshore of Ternate Island is marked with a white triangle B maximum likelihood phylogeny based on the mitochondrial cytochrome c oxidase subunit 1 gene, with strong bootstrap support for four clades within the A. brunnea group. Atlanta vanderspoeli is supported as a valid species, and A. brunnea is formed of two geographically isolated clades. Bootstrap support (%) for nodes is displayed and branch lengths are proportional to the amount of inferred change, as indicated by the scale bar (mean number of nucleotide substitutions per site).
Figure 4 from: Wall-Palmer D, Hegmann M, Goetze E, Peijnenburg KTCA (2019) Resolving species boundaries in the Atlanta brunnea species group (Gastropoda, Pterotracheoidea). ZooKeys 899: 59-84. https://doi.org/10.3897/zookeys.899.38892
Figure 4 Maximum likelihood phylogeny of the A. brunnea species group based on analysis of the combined genes CO1, 28S and 18S with a total alignment of 2447 bp. All four clades within the A. brunnea species group are monophyletic with strong bootstrap support. Bootstrap support (%) for nodes is displayed and branch lengths are proportional to the amount of inferred change, as indicated by the scale bar (mean number of nucleotide substitutions per site).
Figure 10 from: Wall-Palmer D, Hegmann M, Goetze E, Peijnenburg KTCA (2019) Resolving species boundaries in the Atlanta brunnea species group (Gastropoda, Pterotracheoidea). ZooKeys 899: 59-84. https://doi.org/10.3897/zookeys.899.38892
Figure 10 Five specimens of Atlanta turriculata forma B identified by van der Spoel and held in the collection at the Naturalis Biodiversity Center. These specimens are now designated as paratypes of Atlanta vanderspoeli RMNH.MOL.342212.
Figure 1 from: Wall-Palmer D, Hegmann M, Goetze E, Peijnenburg KTCA (2019) Resolving species boundaries in the Atlanta brunnea species group (Gastropoda, Pterotracheoidea). ZooKeys 899: 59-84. https://doi.org/10.3897/zookeys.899.38892
Figure 1 Collection locations for A. brunnea group specimens analysed in this study. Members of this species group are known to inhabit all oceans from 40N to 30S (Wall-Palmer et al. 2018b).
Mānpur मानपुर (रायसेन ज़िला) Madhya Pradesh. Temple, south wall, detail.
<p>Mānpur मानपुर (<a href="https://hi.wikipedia.org/wiki/%E0%A4%B0%E0%A4%BE%E0%A4%AF%E0%A4%B8%E0%A5%87%E0%A4%A8_%E0%A4%9C%E0%A4%BC%E0%A4%BF%E0%A4%B2%E0%A4%BE">रायसेन ज़िला</a>) Madhya Pradesh. Temple, south wall, detail.</p>
Current-driven magnetic domain-wall logic
<p>Open access data set for manuscript Current-driven magnetic domain-wall logic, <a href="https://www.nature.com/nature"><em>Nature</em></a> <strong>volume 579</strong>, pages214–218(2020)</p>
Rapid and sensitive quantification of cellular associated multi-walled carbon nanotubes
<p>Datasets of "Rapid and sensitive quantification of cellular associated multi-walled carbon nanotubes".</p>
Data belonging to the paper"Culm cell-wall compositions of tribes Bambuseae and Olyreae (subfamily Bambusoideae; Family Poaceae) from the Brazilian Atlantic Forest"
<p>The data in the following table (Appendix 1) presents relative areas produced from the integration of the peaks monosaccharides analysed by anion-exchange chromatography followed by integrated pulsed amperometric detection (PAD) from of the cell wall fractionation three biological samples of six Neotropical bamboo species collected</p>
Fig 5 from: Gardiner T, Fargeaud K (2020) Microhabitats of planted sea wall strips used by pollinators and Orthoptera. Journal of Orthoptera Research 29(1): 77-82. https://doi.org/10.3897/jor.29.34452
Fig 5 A teasel (Dipsacus fullonum) flowerhead visited by the tree bumblebee (Bombus hypnorum) in 2019. Photo credit: T. Gardiner.
Fig 3 from: Gardiner T, Fargeaud K (2020) Microhabitats of planted sea wall strips used by pollinators and Orthoptera. Journal of Orthoptera Research 29(1): 77-82. https://doi.org/10.3897/jor.29.34452
Fig 3 Pollinator strip with a short sward ideal for Orthoptera nymphs being planted with plugs by the second author in April 2018. Photo credit: T. Gardiner.
Fig 4 from: Gardiner T, Fargeaud K (2020) Microhabitats of planted sea wall strips used by pollinators and Orthoptera. Journal of Orthoptera Research 29(1): 77-82. https://doi.org/10.3897/jor.29.34452
Fig 4 Roesel's bush-cricket (Roeseliana roeselii) nymph on a planted teasel (Dipsacus fullonum) leaf in 2019. Photo credit: T. Gardiner.
Fig 2 from: Gardiner T, Fargeaud K (2020) Microhabitats of planted sea wall strips used by pollinators and Orthoptera. Journal of Orthoptera Research 29(1): 77-82. https://doi.org/10.3897/jor.29.34452
Fig 2 Principal components for the adult (grasshopper and R. roeselii), sward height/variability, and rabbit grazing data. PC1 represents sward height, PC2 represents R. roeselii adult density.
Fig 1 from: Gardiner T, Fargeaud K (2020) Microhabitats of planted sea wall strips used by pollinators and Orthoptera. Journal of Orthoptera Research 29(1): 77-82. https://doi.org/10.3897/jor.29.34452
Fig 1 Principal components for the nymph (grasshopper and R. roeselii), sward height/variability, and rabbit grazing data. PC1 represents sward height, PC2 represents R. roeselii nymph density.
Figure 2 in The muscles, body wall and valve-opening mechanism of extant craniid (inarticulated) brachiopods
Figure 2. Digital and scanning electron micrographs (SEM) illustrating anatomical features. (A–H) Novocrania californica. (A). SEM of a piece of anterior adductor muscle, showing fibres make up whole length. (B) SEM close-up of fibres in A. (C) Lophophore cut to show brachial muscle and empty hydrostatic skeleton channel. (D) Ventral view of anterior adductor muscle,
Figure 5 in The muscles, body wall and valve-opening mechanism of extant craniid (inarticulated) brachiopods
Figure 5. Line drawings and digital and scanning electron micrographs illustrating organic ventral mounds and lophophore filaments. (A, B) Novocrania lecointei. (A) NIWA 37947. Transparent organic ventral valve with organic ventral mound on dark rock. (B) Cutaway drawing down midline. (C–F) Novocrania anomala. (C) OU 44526a. Ventral valve with organic ventral mound. (D) OU 44525a. Ventral valve with organic mound rotted away. (E) OU 39355. Dorsal valve with muscle scars flush with valve surface. (F) Reproduction of illustration of N. anomala with lophophore filaments extended (from Barrett 1856). All scale bars 2 mm. Abbreviations: aasc, anterior adductor muscle scar; bwi, "batwing" shaped outline of organic ventral valve; dv, dorsal valve; fi, filaments; obisc, oblique internal muscle scar; opab, organic posterior adductor base; ovm, organic ventral mound; ovv, organic ventral valve; pasc, posterior adductor muscle scar; vv, ventral valve.
Cold-water coral assemblages on vertical walls: distribution patterns from the Northeast Atlantic
<p><b>Aim</b>: In this study, we assess patterns of cold-water coral assemblages observed on deep-sea vertical walls. Similar to their shallow-water counterparts, vertical and overhanging walls in the deep sea can host highly diverse communities, but because of their geometry, these habitats are generally overlooked and remain poorly known. These vertical habitats are however of particular interest, because they can protect vulnerable coral ecosystems from trawling activities. As such, it is important to understand their ecology and assess their global importance. </p> <p><b>Location</b>: Vertical walls on complex geomorphic features, in particular walls of the Rockall Bank Slope Failure Escarpment, Whittard and Explorer Canyons, Northeast Atlantic.</p> <p><b>Methods</b>: Video analysis of ROV transects carried out at five sites is used to investigate differences in species composition and diversity across walls and to compare those to nearby cold-water coral sites on flat terrain. A high-resolution photogrammetric reconstruction is further employed to examine whether wall complexity plays a role in promoting niche differentiation at very fine spatial scales. </p> <p><b>Results</b>: The investigated walls showed differences in species assemblage both across walls as well as in comparison to flat sites, with the fine-scale heterogeneity engendered by walls allowing niche differentiation between closely-related taxa. </p> <p><b>Main Conclusions</b>: Vertical walls represent an important cold-water coral habitat with differences in species composition across walls within a region, illustrating their role in driving diversity patterns. Based on publicly available bathymetric datasets and a catalogue of broad-scale terrain features, globally over 8,000 features are likely to have vertical walls and cold-water corals, which highlights the need to consider deep-sea vertical habitats in current conservation efforts.</p>
FIG. 34 in The early 8 century A.D. zoomorphic iconography of the wall decorations in Qasr al-Amra, Hashemite Kingdom of Jordan
FIG. 34. — Detail of a miniature from the Khamsa The motifs of the gazelle scratching its ear with its hind leg is clearly associated with the tale of Bahram Gur (f. 158b; St. Petersburg, Saltikov-Shchedrin Public Library).
FIG. 33 in The early 8 century A.D. zoomorphic iconography of the wall decorations in Qasr al-Amra, Hashemite Kingdom of Jordan
FIG. 33. — Detail of the vault decoration of the Qasr al-Amra tepidarium illus- trating a male gazelle scratching an ear with one of its hind legs (photo by Fabio Vianello).
FIG. 28 in The early 8 century A.D. zoomorphic iconography of the wall decorations in Qasr al-Amra, Hashemite Kingdom of Jordan
FIG. 28. — Detail of the ceiling decoration of the Qasr al-Amra tepidarium illus- trating a marbled polecat curving its tail above its back to eject the contents of its anal glands (from Vibert-Guigue & Bisheh 2007).
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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)
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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.