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78 results for “BEAGLE”
FIG. 6 in Populations of a new morphotype of corrugate Lessonia Bory in the Beagle Channel, sub-Antarctic Magellanic ecoregion: a possible case of on-going speciation
FIG. 6. — MJ network of ITS1 haplotypes of Magellanic Lessonia Bory, spp. individuals.
Genotype likelihood (beagle file) and genotype (vcf) files of North Atlantic and Black Sea Harbour porpoises (Phocoena phocoena)
<p><span>The Harbour porpoise (<em>Phocoena phocoena</em>) is a highly mobile cetacean species primarily occurring in coastal and shelf waters across the Northern hemisphere. It inhabits heterogeneous seascapes broadly varying in salinity and temperature. Here we produced 74 whole genomes at intermediate coverage to study Harbour porpoise's evolutionary history and investigate the role of local adaptation in the diversification into subspecies and populations. We identified ~6 million high-quality SNPs sampled at 8 localities across the North Atlantic </span><span>and adjacent waters</span><span>, which we used for population structure, demographic, and genotype-environment association analyses. Our results suggest a genetic differentiation between three subspecies (<em>P.p. relicta</em>, <em>P.p. phocoena,</em> and the recently proposed <em>P.p meridionalis</em>), and three distinct populations within the subspecies <em>P.p. phocoena</em>: Atlantic, Belt Sea, and Proper Baltic Sea. Effective population size and Tajima's D levels suggest a population contraction in Black Sea and Iberian porpoises, but a population expansion in the <em>P.p. phocoena</em> populations</span><span>. </span><span>Phylogenetic trees</span> <span>indicate a post-glacial colonization from a southern refugium. </span><span>Genotype-environment association analysis identified salinity as a major driver in genomic variation and we identified candidate genes putatively underlying adaptation to different salinity levels. </span><span>Our study highlights the value of whole genome resequencing to unravel subtle population structure in highly mobile species, shows how strong environmental gradients and local adaptation may lead to population differentiation and how neutral and adaptive markers give different perspectives on population subdivision. </span><span>The results have great conservation implications as we found inbreeding and low genetic diversity in the endangered Black Sea subspecies and identified the critically endangered Proper Baltic Sea porpoises as a separate population.</span></p>
Genotype likelihood (beagle file) and genotype (vcf) files of North Atlantic and Black Sea Harbour porpoises (Phocoena phocoena)
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Data from:Investigation of urinary miRNA profile changes in amphotericin B-induced nephrotoxicity in C57BL/6 mouse, Sprague-Dawley rats and beagle dogs
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Heritability and genome-wide association study of vaccine-induced immune response in Beagles: A pilot study
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Data from: Identification of the Beagle 2 lander on Mars
The 2003 Beagle 2 Mars lander has been identified in Isidis Planitia at 90.43° E, 11.53° N, close to the predicted target of 90.50° E, 11.53° N. Beagle 2 was an exobiology lander designed to look for isotopic and compositional signs of life on Mars, as part of the European Space Agency Mars Express (MEX) mission. The 2004 recalculation of the original landing ellipse from a 3-sigma major axis from 174 km to 57 km, and the acquisition of Mars Reconnaissance Orbiter High Resolution Imaging Science Experiment (HiRISE) imagery at 30 cm per pixel across the target region, led to the initial identification of the lander in 2014. Following this, more HiRISE images, giving a total of 15, including red and blue-green colours, were obtained over the area of interest and searched, which allowed sub-pixel imaging using super high-resolution techniques. The size (approx. 1.5 m), distinctive multilobed shape, high reflectivity relative to the local terrain, specular reflections, and location close to the centre of the planned landing ellipse led to the identification of the Beagle 2 lander. The shape of the imaged lander, although to some extent masked by the specular reflections in the various images, is consistent with deployment of the lander lid and then some or all solar panels. Failure to fully deploy the panels—which may have been caused by damage during landing—would have prohibited communication between the lander and MEX and commencement of science operations. This implies that the main part of the entry, descent and landing sequence, the ejection from MEX, atmospheric entry and parachute deployment, and landing worked as planned with perhaps only the final full panel deployment failing.
Figure 23 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 23. Ensayara gappai sp. nov. Holotype, ovigerous female: (A) lateral view; (B) head; (C, D) antennae 1, 2; (E) upper lip; (F, G) right and left mandibles; (H) mandibular palp. Scale bars: a: (A) 1 mm; b: (B) 0.2 mm; c: (C, D), d: (E–H) 0.1 mm.
Figure 21 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 21. Erikus lovrichi sp. nov. Paratype, male 13 mm: (A) lateral view; (B) antenna 1; (C) callynophore; (D) antenna 2; (E) antenna 2 peduncle. Scale bars: a: (A) 3 mm; b: (B, D) 0.5 mm; c: (C), d: (E) 0.2 mm.
Figure 19 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 19. Erikus lovrichi sp. nov. Holotype, ovigerous female: (A) gnathopod 2; (B, C) gnathopod 2 palms; (D) peraeopod 3; (E) peraeopod 3 coxa ventrodistal margin; (F) peraeopod 3 dactyluds; (G–J) peraeopods 4–7. Scale bars: a: (A, D, G–J) 0.5 mm; b: (B, C) 0.1 mm; c: (E, F) 0.2 mm.
Figure 25 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 25. Ensayara gappai sp. nov. Holotype, ovigerous female: (A) gnathopod 2; (B) gnathopod 2 propodus; (C) peraeopod 3; (D) peraeopod 3 propodus; (E, F) peraeopods 4, 5. Scale bars: a: (A, C, F), c: (E) 0.2 mm; b: (B, D) 0.1 mm.
Figure 17 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 17. Erikus lovrichi sp. nov. Holotype, ovigerous female: (A) antenna 1; (B) antenna 1 peduncle; (C) antenna 1 peduncle article 1; (D) antenna 2; (E) epistome; (F) right mandible; (G) left lacinia mobilis; (H) right setal row; (I, J) right and left mandibular palp. Scale bars: a: (A, D) 0.5 mm; b: (B), e: (F) 0.2 mm; c: (C), d: (E, G–J) 0.1 mm.
Figure 33 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 33. Heterophoxus despard sp. nov. Holotype, ovigerous female: (A–C) peraeopods 5–7; (D) pleopod 3; (E) epimera 1–3. Scale bars: a: (A, C, D), b: (B), c: (E) 0.2 mm.
Figure 28 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 28. Lysianopsis ona sp. nov. Holotype, ovigerous female: (A) lower lip; (B) maxilla 1; (C) maxilla 1 outer plate; (D) maxilla 2; (E) maxilliped; (F) gnathopod 1; (G) gnathopod 1 dactylus; (H) gnathopod 2; (I) gnathopod 2 propodus. Scale bars: a: (A, B, D, E, I), d: (G) 0.1 mm; b: (C) 0.025 mm; c: (F), e: (H) 0.2 mm.
Figure 6 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 6. Ventojassa beagle sp. nov. Holotype, ovigerous female: (A) head; (B) antenna 2; (C) antenna 2 last article; (D) upper lip; (E) epistome; (F, G) right and left mandibles. Scale bars: a: (A, B) 0.2 mm; b: (C) 0.05 mm; c: (D–G) 0.025 mm.
Figure 1 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 1. Aora parda sp. nov. Holotype, male: (A) head; (B) upper lip; (C, D) right and left mandibles; (E) mandibular palp; (F) lower lip; (G, H) maxillae 1, 2. Scale bars: a: (A) 0.2 mm; b: (B–H) 0.1 mm.
Figure 7 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 7. Ventojassa beagle sp. nov. Holotype, ovigerous female: (A) mandibular palp; (B) lower lip; (C) maxilla 1; (D) maxilla 1 palp; (E) maxilla 2; (F) maxilliped; (G, H) maxilliped inner and outer plates; (I) maxilliped dactylus. Scale bars: a: (A, C, E, G–I), b: (B), c: (D) 0.025 mm; d: (F) 0.05 mm.
Figure 10 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 10. Ventojassa beagle sp. nov. Holotype, ovigerous female: (A, B) uropods 2, 3; (C) uropod 3 rami; (D) telson. Paratype, ovigerous female 3.6 mm: (E) lateral view. Paratype, ovigerous female 4 mm: (F) antenna 1; (G) antenna 1 flagellum. Scale bars: a: (A, B, G) 0.05 mm; b: (C), c: (D) 0.025 mm; d: (E) 1 mm; e: (F) 0.2 mm.
Figure 13 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 13. Oradarea surera sp. nov. Holotype, ovigerous female: (A) mandibular palp; (B) lower lip; (C, D) maxillae 1, 2; (E) maxilliped; (F) gnathopod 1; (G) gnathopod 1 palm. Scale bars: a: (A, C–E), b: (B), d: (G) 0.1 mm; c: (F) 0.2 mm.
Figure 5 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 5. Aora parda sp. nov. Paratype, ovigerous female 8 mm: (A) gnathopod 1; (B) gnathopod 1 dactylus; (C) gnathopod 2; (D) gnathopod 2 dactylus. Scale bars: a: (A, C) 0.2 mm; b: (B, D) 0.05 mm.
Figure 32 in Amphipod crustaceans (Corophiidea and Gammaridea) associated with holdfasts of Macrocystis pyrifera from the Beagle Channel (Argentina) and additional records from the Southwestern Atlantic
Figure 32. Heterophoxus despard sp. nov. Holotype, ovigerous female: (A) maxilliped; (B, C) maxilliped inner and outer plates; (D) gnathopod 2; (E) peraeopod 3; (F) peraeopod 3 propodus; (G) peraeopod 4. Scale bars: a: (A–C, F) 0.1 mm; b: (D, E, G) 0.2 mm.
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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.