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FIGURE 10 in Alyxia Banks ex R.Br. in New Caledonia: a clarification of several species complexes, nomenclatural notes, and a description of three new species
FIGURE 10. Known distribution Alyxia minimiflora(dots) and Alyxia nummularia (squares). Symbols with "T" represent type specimens. Grayed areas represent ultramafic substrates.
Fig. 4 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 4. Axis of CVA under aquatic environment approach with ellipses of the probability of 95%, and the grid of morphometric space of CVA with a factor of deformation ¼ 0.1; (A) axis 1 of CVA and (B) axis 2 of CVA.
Fig. 3. CVA 1 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 3. CVA 1 vs. CVA 2 by population at geometric morphometric space delimited by minimum convex polygons, and the grid of morphometric space of CVA with a factor of deformation ¼ 0.1; (A) axis 1 of CVA and (B) axis 2 of CVA.
Fig. 1 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 1. Study area, Yucatan Peninsula. Localities of M. urophthalmus taken into account for the geometric morphometric analysis, in gray numbers. Localities with genetic data, marked with an asterisk. Localities from nominal species included in the morphometric analysis: M. alborus (15), M. cienagae (10), M. conchitae (8), M. mayorum (6), and M. zebra (9).
Fig. 2 in Several Subspecies or Phenotypic Plasticity? A Geometric Morphometric and Molecular Analysis of Variability of the Mayan Cichlid Mayaheros urophthalmus in the Yucatan
Fig. 2. Constellation of landmarks and semilandmarks for the geometric morphometric analysis showing Procrustes superimposition of landmarks and semilandmarks. Anatomical positions of landmarks: Landmark 1—intersection between the posterior base of dorsal fin and caudal peduncle; Landmark 2—the most distal pore of the end of lateral line; Landmark 3—intersection between the posterior base of the pelvic fin and caudal peduncle; Landmark 4—intersection between anterior base of pelvic fin and belly; Landmark 5—apical intersection between subopercle and interopercle; Landmark 6—commissure of dentary at the more posterior end at its junction with the anguloarticular, quadrates, and ectometapterygoid bone; Landmarks 7 and 8—delimitation of the width of the commissure of dentary at its junction with the maxilla; Landmarks 9 and 10—delimitation of the width of the dentary at the more anterior end; Landmarks 10 and 12—delimitation of the width of the premaxilla at the more anterior end; Landmark 11—dorsal end of edge between opercle and cheek; Landmarks 12 to 24—the curve of 13 semilandmarks beginning at the intersection between the premaxilla and ascending process at semilandmark 12, the curve traced upwards until the base of dorsal fin at semilandmark 24.
Dataset of "Exploring the Landscape and Severity of Distributed Denial of Service Attacks"
<p>The Internet of Things and Operational Technology technologies allow the Internet to be connected to a wide range of devices. The use of the Internet not only enables the management of these connected devices and the transmission of information through various devices but also exposes them to security threats. These threats include, but are not limited to, Denial of Service (DoS) attacks. Some attacks target specific types of devices, services, or web server versions. In this paper, we have enumerated and compared the most well-known (D)DoS attacks. Our paper provides a wide area of (D)DoS attacks sorted by ISO/OSI layers. Each listed attack is described, detection and mitigation techniques are presented, and a simulation tool capable of generating attacks is also presented. In total, we have focused on 46 attacks. In addition, a simulation of selected DoS, DDoS, and slow DoS attacks is carried out in an experimental setup workstation, and the impacts are compared.</p>
Comparison-adjusted Funnell plots for the Primary outcomes: Treatment Failure, Endotracheal Ventilation and Moderate-Severe CLD
<p>Supplementary File #10 for Cochrane review entitled: "Non-invasive respiratory support in preterm infants as primary mode: a network meta-analysis"</p>
FIGURE 4 in A new species of the Cambeva variegata group (Siluriformes: Trichomycteridae) from the Serra do Espinhaço, south-eastern Brazil, under severe risk of extinction
FIGURE 4. Biotopes of Cambeva damnata sp. nov. in (a,b) Córrego do Jambreiro, Município de Nova Lima, (c,d) Ribeirão da Prata, Município de Raposos: (a, c) out of water general view; (b,d) underwater view.
FIGURE 3 in A new species of the Cambeva variegata group (Siluriformes: Trichomycteridae) from the Serra do Espinhaço, south-eastern Brazil, under severe risk of extinction
FIGURE 3. Geographical distribution of the Cambeva variegata species group: (1) Cambeva concolor (Costa, 1992); (2) Cambeva variegata (Costa, 1992); (3) Cambeva damnata sp. nov. Stars indicate type localities.
FIGURE 1 in A new species of the Cambeva variegata group (Siluriformes: Trichomycteridae) from the Serra do Espinhaço, south-eastern Brazil, under severe risk of extinction
FIGURE 1. Cambeva damnata sp. nov., holotype, UFRJ 7026, 12967, 46.5 mm SL. (a) lateral view; (b) dorsal view; (c) ventral view.
FIGURE 2 in A new species of the Cambeva variegata group (Siluriformes: Trichomycteridae) from the Serra do Espinhaço, south-eastern Brazil, under severe risk of extinction
FIGURE 2. Ontogenetic variation of colouration in Cambeva damnata sp. nov., paratypes, UFRJ 12983: (a) 20.9 mm SL; (b) 21.4; (c) 28.3; (d) 30.7; (e) 33.9 mm SL; (f) 43.2 mm SL; (g) 44.3 mm SL; (h) 53.5 mm SL.
FIGURE 1. Scleria pantadenia.—A. Habit.—B. Glomerule with several spikelets.—C. Nutlet.—D in Scleria pantadenia and Scleria tricristata: Two new species of Scleria subgenus Hypoporum (Cyperaceae, Cyperoideae, Sclerieae) from Tanzania
FIGURE 1. Scleria pantadenia.—A. Habit.—B. Glomerule with several spikelets.—C. Nutlet.—D. Schematic overview of a glomerule.— E. Diagram of glomerule with detail of spikelet diagram. From the type specimen S. Bidgood et al. 5550 (MO). Br = gomerula bract; g = glume; p = prophyll; x = represents two stamens.
FIGURE 2. Scleria tricristata.—A. Habit.—B. Glomerule with several spikelets.—C in Scleria pantadenia and Scleria tricristata: Two new species of Scleria subgenus Hypoporum (Cyperaceae, Cyperoideae, Sclerieae) from Tanzania
FIGURE 2. Scleria tricristata.—A. Habit.—B. Glomerule with several spikelets.—C. Detail of glume surface.—D. Nutlet.—E. Schematic overview of a glomerule.—F. Diagram of glomerule with detail of spikelet diagram. From the type specimen S. Bidgood et al. 6083 (MO). Br = spikelet bract; g = glume; p = prophyll; x = represents two stamens.t
FIGURE 2 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 2. Neighbour net analysis of nrITS sequences. The main clusters are shaded in color; (grey) A-genome diploids and Asian tetraploid C. sosnowskyi; (green) Eurasian diploids (B-genome), American and Asian tetraploids and Taiwan hexaploid C. formosanum; (yellow) two Asian diploids; (red) Asian diploid (C. acuminatum) and most of the Asian and Eurasian polyploids. Bootstrap values>80% are given only for the major groups of the analyzed accessions.
FIGURE 3 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 3. Neighbour net analysis of 5S rDNA NTS sequences. The main clusters are shaded in color; (grey) sequences from A-genome diploids and American allotetraploids; (green) sequences from Eurasian diploids (B-genome), American allotetraploids and all analyzed hexaploid; (red) sequences from Eurasian tetraploids (C. betaceum, C. striatiforme) and two Eurasian hexaploids; (orange) sequences of Eurasian tetraploids (C. betaceum, C. striatiforme) and three Eurasian hexaploids. Bootstrap values>80% are given only for the major groups of the analyzed accessions.
FIGURE 1 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 1. Neighbour net analysis of cpDNA sequences. The main clusters are shaded in color; (grey) A-genome diploids and American allotetraploids with AABB genome composition; (red) Eurasian tetraploids (C. betaceum and C. striatiforme) and Eurasian hexaploid species (C. pedunculare, C. album and C. giganteum); (green) Eurasian diploids (B-genome) and Taiwan hexaploid C. formosanum. Bootstrap values>80% are given only for the major groups of the analyzed accessions.
FIGURE 6 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 6. Evolution of rDNA loci and genome size in allohexaploids C. album, C. giganteum, C. pedunculare, C. formosanum and C. opulifolium. Putative diploid and tetraploid ancestors are indicated by green and grey arrows, respectively. Genome size (1C), subgenome B (green), chromosome carrying 35S (yellow), or 5S (magenta) loci and their putative provenance (♂ for paternal and ♀ for maternal parent), as well as a type of ITS and 5S rDNA non-transcribed spacer (NTS) sequences (♂ for paternal and ♀ for maternal parent) are shown.
FIGURE 4 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 4. Somatic metaphases of (a) C. album (BGG 4356), (b) C. pedunculare, (c) C. giganteum (PI 596372), (d) C. formosanum and (e) C. opulifolium after double GISH with gDNA isolated from C. ficifolium (green) and tetraploid C. betaceum (red). The scale bar=5 μm.
FIGURE 5 in Parental origin and genome evolution of several Eurasian hexaploid species of Chenopodium (Chenopodiaceae)
FIGURE 5. Distribution of 35S (yellow) and 5S rDNA (magenta) loci in chromosomes of Chenopodium species; (a) C. betaceum; (b) C. striatiforme; (c) C. giganteum (IPK Chen61), (d) C. pedunculare. Somatic metaphases of (e) C. album (UHBG 36), (f) C. pedunculare, (g) C. formosanum, (h–i) C. giganteum (PI 596372) and (j) C. opulifolium after GISH/FISH with gDNA isolated from C. ficifolium (green), 35S rDNA (yellow) and 5S rDNA (magenta). The scale bar=5 μm.
Dataset to several methods for assessment of research waste: a scoping review
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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.