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13,017 results for “Positionning”
Figure 3 from: Ezzine IK, Pfarrer B, Dimassi N, Said K, Neubert E (2017) At home at least: the taxonomic position of some north African Xerocrassa species (Pulmonata, Geomitridae). ZooKeys 712: 1-27. https://doi.org/10.3897/zookeys.712.13066
Figure 3 - Anatomy of genital organs of Xerocrassa latasteopsis; A X. latasteopsis, NMBE 551301, Henchir el Zitouna: situs, penial lumen and atrial lumen B X. latasteopsis NMBE 549906, Sidi Aich 2, situs, penial lumen; and atrial lumen.
Figure 1 from: Ezzine IK, Pfarrer B, Dimassi N, Said K, Neubert E (2017) At home at least: the taxonomic position of some north African Xerocrassa species (Pulmonata, Geomitridae). ZooKeys 712: 1-27. https://doi.org/10.3897/zookeys.712.13066
Figure 1 - Anatomy of genital organs of Xerocrassa latastei; Jorf, 6.12.2015, leg. Ezzine, NMBE 549907/1; A situs B atrium. Abbreviations: a = atrium; al = atrial lumen; ds = dart sac(s); ep = epiphallus; fl = flagellum; gm = glandulae mucosae; itc = internal tissue cone; mrp = penial retractor muscle; p = penis; ped = pedunculus; po = pore of penial papilla; pp = penial papilla; sod = spermoviduct; sti = stimulator (?); vd = vas deferens.
Figure 9 from: Ezzine IK, Pfarrer B, Dimassi N, Said K, Neubert E (2017) At home at least: the taxonomic position of some north African Xerocrassa species (Pulmonata, Geomitridae). ZooKeys 712: 1-27. https://doi.org/10.3897/zookeys.712.13066
Figure 9 - Phylogenetic trees obtained by Bayesian inference (BI) and Maximum Likelihood (ML) methods. A Tree inferred based on partial mitochondrial sequences of COI and 16S B Tree inferred based on mitochondrial data, partial sequences of 5.8S, complete sequence of ITS2 and partial sequence of 28S rRNA. Posterior probability (PB) obtained from Bayesian analysis and bootstrap values obtained from Maximum likelihood (ML) were presented on each node (*: BS= 100).
Figures 4-7 from: Ezzine IK, Pfarrer B, Dimassi N, Said K, Neubert E (2017) At home at least: the taxonomic position of some north African Xerocrassa species (Pulmonata, Geomitridae). ZooKeys 712: 1-27. https://doi.org/10.3897/zookeys.712.13066
Figures 4-7 - Xerocrassa species. 4 Xerocrassa latastei, lectotype MHNG-MOLL 115121, Ketenna [= Kettana], D = 15.9 mm 5 Xerocrassa latasteopsis, lectotype MHNG-MOLL 115131, Foum Hallouf, D = 18.34 mm 6 Xerocrassa latasteopsis, NMBE 549906, Sidi Aich 2, D = 18.2 mm 7 Xerocrassa lacertara, syntype MHNG-MOLL 114001, "Plaines entre Djelfa et El-Aghouat", D = 11.8 mm.
THE POSITION OF LANGUAGE UNITS EXPRESSING THE CATEGORY OF ADDRESS IN THE LANGUAGE SYSTEM
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Dataset for the paper: Predicting protein functions using positive-unlabeled ranking with ontology-based priors
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Figure S1: SARS-CoV-2-specific neutralization activity at days 1 and 8 relative to enrollment in exposed seronegative nasal SIgA positive and infected participants.
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FIGURE 6 in Description and phylogenetic position of a new species of Rhyacoglanis (Siluriformes: Pseudopimelodidae) from the Jamanxim River basin
FIGURE 6 | The type locality of Rhyacoglanis beninei in córrego Jussara, 07°21'08"S 55°17'45"W (yellow star), Tapajós River basin.
FIGURE 1 in Phylogenetic position of Kinnareemimus khonkaenensis (Dinosauria: Theropoda: Ornithomimosauria) from the Lower Cretaceous of Thailand
FIGURE 1. Skeleton (A) and life (B) reconstruction of Kinnareemimus khonkaenensis ©Wijanee Sendang.
Simulation data for "Modeling radiation belt dynamics using a positivity-preserving finite volume method on general meshes"
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WAYS TO ENSURE THE STABILITY OF THE FINANCIAL POSITION OF COMMERCIAL BANKS IN THE REPUBLIC OF TAJIKISTAN
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FIGURE 12 in Identifying tooth position of isolated teeth of sparassodonts (Mammalia: Metatheria) using geometric morphometrics
FIGURE 12. Plot of the first two canonical variates (CVs) of the reduced taxon (no Tiupampa taxa, borhyaenids, or thylacosmilids), trigon-only discriminant analysis with tooth locus coded by symbol and incorrectly-classified specimens uncolored. Convex hulls represent morphospace occupied by each tooth locus.
Figs. 10-14 in Dorsal chaetotaxy of neotropical species supports a basal position for the genus Lepidonella among scaled Paronellidae (Collembola, Entomobryoidea)
Figs. 10-14. Lepidonella zeppelinii sp. nov.; (10) Dorsal chaetotaxy of abdomen 4; (11) Trochanteral organ; (12) Metathoracic claw complex; (13) Dens and mucro; (14) Detail of mucro.
Figures 29-40 in The systematic position of the scorpion genera Heteroscorpion Birula, 1903 and Urodacus Peters, 1861 (Scorpiones: Scorpionoidea)
Figures 29-40: Chelicerae, dorsal view, of representative genera of families Hemiscorpiidae and Scorpionidae showing the differences between the two families in the relative sizes of the ventral and dorsal distal denticles and the size of the subdistal (sd) denticle of the movable finger. 29. Heteroscorpion raselimananai, female holotype. 30. Heteroscorpion goodmani, male paratype. 31. Hadogenes troglodytes. 32. Opisthacanthus asper. 33. Liocheles karschii. 34. Opisthacanthus lepturus. 35. Urodacus elongatus. 36. Urodacus yaschenkoi. 37. Heterometrus swammerdami. 38. Scorpio maurus. 39. Opistophthalmus pugnax. 40. Nebo hierichonticus.
Fig. 4 in Cranial anatomy and phylogenetic position of the titanosaurian sauropod Bonitasaura salgadoi
Fig. 4. Photographs and interpretive drawings of the titanosauroid Bonitasaura salgadoi Apesteguía, 2004 from the Upper Neuquén Group of Río Negro province, Patagonia, MPCA 460. Left quadrate in anterior (A), medial (B), posterior (C), and lateral (D) views.
Fig. 3 in Cranial anatomy and phylogenetic position of the titanosaurian sauropod Bonitasaura salgadoi
Fig. 3. Photographs and interpretive drawings of the titanosauroid Bonitasaura salgadoi Apesteguía, 2004 from the Upper Neuquén Group of Río Negro province, Patagonia, MPCA 460. Right lacrimal in anterior (A), lateral (B), posterior (C), and medial (D) views.
Fig. 3 in New skeleton from the early Oligocene of Germany indicates a stem-group position of diomedeoidid birds
Fig. 3. Stratigraphy of the Rheinweiler locality. Note that the layers containing the bird are situated at about 1.5 m, between the samples RW17 and RW18 (shown in bold).
◂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
Photosynthesis Capacity of Isodon rubescens (Hemsley) H. Hara Leaves at different Leaf Positions
<p>The paraffin section of I. rubescens stem peeled due to ice ribbons</p>
Figure 1 from: Zhou L-W, Wang X-W, Vlasák J, Ren G-J (2018) Resolution of phylogenetic position of Nigrofomitaceae within Hymenochaetales (Basidiomycota) and Nigrofomes sinomelanoporus sp. nov. (Nigrofomitaceae) from China. MycoKeys 29: 1-13. https://doi.org/10.3897/mycokeys.29.21250
Figure 1 Phylogenetic position of Nigrofomitaceae inferred from the nLSU dataset. The topology is generated from the maximum likelihood analysis along with bootstrap values (above 50%) and Bayesian posterior probabilities (above 0.8), respectively, calculated from the maximum likelihood and Bayesian inference analyses at the nodes. Newly sequenced specimens are in boldface.
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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.