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2,214 results for “Walls”
Leycesteria formosa Wall. (BR0000009354685)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
FREE Ruined Wall [3D Scan]
Ruined wall free model. Source: Objaverse 1.0 / Sketchfab
Stone Wall in Yanaka: 谷中の石垣
📍 [台東区, 東京都](https://scaniver.se/L35.72136,139.76521) Source: Objaverse 1.0 / Sketchfab
Figure 2 from: Kuramitsu K, Kosaki A, Ishihara T, Yamada H, Watanabe K (2016) Infestation of the woodwasp Tremex apicalis Matsumura (Hymenoptera, Siricidae) on the large-leaf dogwood Swida macrophylla (Wall.) with biological notes on its parasitoid wasps. Journal of Hymenoptera Research 52: 71-79. https://doi.org/10.3897/jhr.52.10060
Figure 2 - Hymenopteran insects landing on and inserting their ovipositor into the Swida macrophylla tree trunk. a Tremex apicalis female b Tremex apicalis ovipositor with abdomen inserted into the wood c Ibalia japonica female d Megarhyssa jezoensis. female. Scale lines = 10 mm.
Figure 4 from: Kuramitsu K, Kosaki A, Ishihara T, Yamada H, Watanabe K (2016) Infestation of the woodwasp Tremex apicalis Matsumura (Hymenoptera, Siricidae) on the large-leaf dogwood Swida macrophylla (Wall.) with biological notes on its parasitoid wasps. Journal of Hymenoptera Research 52: 71-79. https://doi.org/10.3897/jhr.52.10060
Figure 4 - Hymenopteran insects found in Swida macrophylla. a Tremex apicalis prepupa b pupa of Tremex apicalis female c Ibalia japonica pupa d pupa of Megarhyssa sp.1 female. Scale lines = 10 mm.
Figure 1 from: Kuramitsu K, Kosaki A, Ishihara T, Yamada H, Watanabe K (2016) Infestation of the woodwasp Tremex apicalis Matsumura (Hymenoptera, Siricidae) on the large-leaf dogwood Swida macrophylla (Wall.) with biological notes on its parasitoid wasps. Journal of Hymenoptera Research 52: 71-79. https://doi.org/10.3897/jhr.52.10060
Figure 1 - Infested Swida macrophylla at Botanical Garden, University of Tsukuba, Honshu, Japan. a a decayed Swida macrophylla infested with Tremex apicalis b Tremex apicalis adults and their emergence holes (red arrows) on the tree trunk. Scale lines = (a) 100 cm; (b) 100 mm.
Figure 3 from: Kuramitsu K, Kosaki A, Ishihara T, Yamada H, Watanabe K (2016) Infestation of the woodwasp Tremex apicalis Matsumura (Hymenoptera, Siricidae) on the large-leaf dogwood Swida macrophylla (Wall.) with biological notes on its parasitoid wasps. Journal of Hymenoptera Research 52: 71-79. https://doi.org/10.3897/jhr.52.10060
Figure 3 - Swida macrophylla wood infested with Tremex apicalis. a Wood discoloration in the cross section with Tremex apicalis infestation b Basidiocarp of Cerrena unicolor in the wood infested with Tremex apicalis c Longitudinal section through stem of the wood infested with Tremex apicalis and woodwasp larvae, pupae and larval tunnels. Scale lines = (a, c) 100 mm; (b)10 mm.
The effective transmissivity of a plane-walled fracture with circular cylindrical obstacles - dataset for JGR SE manuscript
<p>The data needed to reproduce the figures from the article "The effective transmissivity of a plane-walled fracture with circular cylindrical obstacles" - to be published in JGR SE.</p> <p>The data are provided in vtk (Paraview) or mat (Matlab) format. To the all mat-files are provided scripts (m-files, i.e. figXX_plot.m) to plot the figures.</p>
EC-t dataset for: Using Inverse Gaussian Distribution for Analysis of Breakthrough Curves in Tracer Tests for Sandy Samples in Rigid Wall Cell
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Fast domain-wall and skyrmion logic in a chirally coupled ferrimagnet
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◂Fig. 1 Live photos and dissection of parasitized Aphrodita longipalpa and Veneriserva pygoclava. A Ventral view of A. longipalpa. B Dorsal view of A. longipalpa with removed feltage chaetae, revealing the parasite visible through the body wall. C Ventrally dissected A. longipalpa, exposing the sizable female parasite. Veneriserva pygoclava individuals within the host are indicated by arrowheads. D Juvenile female V. pygoclava, with developing oocytes visible through the body wall along the mid-dorsal orange line. E Female V. pygoclava showing the mid-dorsal orange pigmentation and the white mark at the base of the prostomium. F Male V. pygoclava. G A large female and smaller male V. pygoclava, extracted from the same host. The pygidium is club-shaped in both males and females and juveniles. H Juvenile V. pygoclava shown from multiple angles, characterized by a complete white coloration; black jaws are magnified in panel in Hardly Venus's servant-morphological adaptations of Veneriserva to an endoparasitic lifestyle and its phylogenetic position within Dorvilleidae (Annelida)
◂Fig. 1 Live photos and dissection of parasitized Aphrodita longipalpa and Veneriserva pygoclava. A Ventral view of A. longipalpa. B Dorsal view of A. longipalpa with removed feltage chaetae, revealing the parasite visible through the body wall. C Ventrally dissected A. longipalpa, exposing the sizable female parasite. Veneriserva pygoclava individuals within the host are indicated by arrowheads. D Juvenile female V. pygoclava, with developing oocytes visible through the body wall along the mid-dorsal orange line. E Female V. pygoclava showing the mid-dorsal orange pigmentation and the white mark at the base of the prostomium. F Male V. pygoclava. G A large female and smaller male V. pygoclava, extracted from the same host. The pygidium is club-shaped in both males and females and juveniles. H Juvenile V. pygoclava shown from multiple angles, characterized by a complete white coloration; black jaws are magnified in panel
Fig. 4. Canda pecten Thornely, 1907. A. zooids and avicularia. B. lateral walls. C. opesia and spines. D in Taxonomic study on bryozoans - new additions to the Korean fauna and new species of Petraliella from Seogwipo waters of Jeju Island
Fig. 4. Canda pecten Thornely, 1907. A. zooids and avicularia. B. lateral walls. C. opesia and spines. D. ovicells. Scale bars: 100 μm (AD).
Figure 1 in Range extension and morphology of the Italian wall lizard, Podarcis siculus (Rafinesque-Schmaltz, 1810) (Squamata: Lacertidae), from Turkey
Figure 1. The current distribution of P. siculus in Turkey. Circles show the known records of the literature cited in the text, and squares indicate Gelibolu and Atakum.
Fig. 4 in Puzzle-like Cyst Wall in Centrohelid Heliozoans Raphidiophrys heterophryoidea and Raineriophrys erinaceoides
Fig. 4. Raphidiophrys heterophryoidea. Scanning electron micrographs of air-dried excysted individuals. A – second type cyst scale; view from the concave side; B – group of interconnected second type cyst scales; C – cyst scales of both types; D – group of interconnected second type scales, underlayed with a layer of first type scales; E–I – individual second type cyst scales; J – individual first type cyst scale. * – secondary septa. Scale bars: 2 μm.
FIGURE 2 in Onosma dolichoutum W.T.Wang (Boraginaceae), a new synonym of O. bracteatum Wall.
FIGURE 2. Distribution map of O. dolichoutum and O. bracteatum
Figure 1 in Rediscovery of Ilex excelsa (Wall.) Voigt (Aquifoliaceae) in Western Himalaya after 64 years
Figure 1. Location map showing the distribution of Ilex excelsa in Kathu (Billawar) Jammu Kashmir.
Radiographic, CT and anatomical dorsal hoof wall measurements
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Rice genome-scale network integration reveals transcriptional regulators of grass cell wall synthesis
<p><span><span><span><span><span><span><span><span><span><span><span>Grasses have evolved distinct cell wall composition and patterning relative to dicotyledonous plants. However, despite the importance of this plant family, transcriptional regulation of its cell wall biosynthesis is poorly understood. To identify grass cell wall-associated transcription factors, we constructed the Rice Combined mutual Ranked Network (RCRN). The RCRN covers >90% of annotated rice (<i>Oryza sativa</i>) genes, is high quality, and includes most grass-specific cell wall genes, such as mixed-linkage glucan synthases and hydroxycinnamoyl acyltransferases. Comparing the RCRN and an equivalent <i>Arabidopsis </i>network suggests that grass orthologs of most genetically verified eudicot cell wall regulators also control this process in grasses, but some vary significantly in network connectivity between these divergent species. Reverse genetics, yeast-one-hybrid, and protoplast-based assays reveal that OsMYB61a activates a grass-specific acyltransferase promoter, which confirms network predictions and supports grass-specific cell wall synthesis genes being incorporated into conserved regulatory circuits. In addition, 10 of 15 tested transcription factors, including six novel <u>w</u>all-<u>a</u>ssociated regulators (WAP1, WACH1, WAHL1, WADH1, OsMYB13a, and OsMYB13b), alter abundance of cell wall-related transcripts when transiently expressed. The results highlight the quality of the RCRN for examining rice biology, provide insight into the evolution of cell wall regulation, and identify network nodes and edges that are possible leads for improving cell wall composition.</span></span></span></span></span></span></span></span></span></span></span></p>
Don't judge a lizard by its colour: no evidence for differential socio-sexual behaviour and space use in the colour morphs of the European common wall lizard (Podarcis muralis)
Explaining the evolutionary origin and maintenance of colour polymorphisms is a major challenge in evolutionary biology. Such polymorphisms are commonly thought to reflect the existence of alternative behavioural or life-history strategies under negative frequency-dependent selection. The European common wall lizard Podarcis muralis exhibits a striking ventral colour polymorphism that has been intensely studied and is often assumed to reflect alternative reproductive strategies, similar to the iconic "rock-paper-scissors" system described in the North American lizard Uta stansburiana. However, available studies so far have ignored central aspects in the behavioural ecology of this species that are crucial to assess the existence of alternative reproductive strategies. Here we try to fill this gap by studying the social behaviour, space use, and reproductive performance of lizards showing different colour morphs, both in a free-ranging population from the eastern Pyrenees and in ten experimental mesocosm enclosures. In the natural population, we found no differences between morphs in site-fidelity, space use or male-female spatial overlap. Likewise, colour morph was irrelevant to socio-sexual behaviour, space use, and reproductive success within experimental enclosures. Our results contradict the commonly held hypothesis that P. muralis morphs reflect alternative behavioural strategies, and suggest that we should instead turn our attention to alternative functional explanations.
Figure 12 in New organic-walled Foraminifera (Protista) from the ocean's deepest point, the Challenger Deep (western Pacific Ocean)
Figure 12. Resigella bilocularis sp. nov. Scanning electron micrographs. A, general view; note collapsed initial chamber. B, detail of same specimen showing agglutinated coating of organic wall; note that the grains become more prominent towards proximal part of chamber. C–H, damaged specimen; the initial chamber has been lost. C, general view; areas within boxes are shown in more detail in E–H. D, surface of proximal part of chamber showing agglutinated grains. E, surface towards posterior end of chamber showing agglutinated grains and smoother, intervening areas; box indicates area shown in detail in F. F, detail of organic wall with mesh-like structures and a few flat areas. G, H, surface towards distal part of chamber showing smooth, flake-like features separated by areas with a fine, mesh-like structure. The flake-like features in F–H are probably clay particles.
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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)
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.