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1,544 results for “spots”
Figure 5 in Species delimitation based on multiple criteria: the Spotted Bush Warbler Bradypterus thoracicus complex (Aves: Megaluridae)
Figure 5. Altitudinal distributions of thoracicus/ przevalskii and davidi at three localities in central China where these two groups have been found in sympatry. Includes observations by T. E. Ortvad and J. S. Hansen (in litt.).
Figure 3 in Species delimitation based on multiple criteria: the Spotted Bush Warbler Bradypterus thoracicus complex (Aves: Megaluridae)
Figure 3. Sonograms of songs: A, thoracicus Emei Shan, Sichuan, China, early May; B, przevalskii Mengda, Qinghai province, China, mid-June; C, kashmirensis Manali, Himachal Pradesh, India, late June; D, suschkini Listvyanka, Lake Baikal, Russia, June; E, davidi Huzong, Heilongjiang province, China, late June; F, davidi Jiuzhaigou, Gansu province, China, mid-June. All recordings by Per Alström.
How to collect dried blood spot samples for hepatitis C testing (Spanish: Cómo obtener muestras de gota de sangre seca para el cribado de la hepatitis C)
<p>Short video in Spanish describing how to collect, store and ship to the laboratory, dried blood spot (DBS) samples for hepatitis C virus (HCV) testing.</p> <p>With proper training of the staff involved, DBS samples can be collected outside the healthcare setting, thus facilitating access to diagnosis of hepatitis C by the most vulnerable populations who attend different centers in the community.<br> With our experience in detecting HCV RNA from DBS samples since 2015, we have produced an explanatory video and a booklet with step-by-step instructions on how to obtain good quality DBS samples for laboratory HCV testing.<br> DBS samples not only allow us to improve the diagnosis rate of viremic HCV infection, but also to monitor the elimination of hepatitis C. Within the following website you can see the publications of different studies that we have carried out using DBS, which have also helped us to characterize the HCV epidemic at the local level.</p> <p>https://www.researchgate.net/project/Development-and-assessment-of-alternative-testing-strategies-for-the-detection-of-active-hepatitis-C-virus-infection-among-vulnerable-groups-at-risk-and-micro-elimination/update/61011c48647f3906fc8c31b8</p> <p> </p>
Data from: Tall, heterogenous forests improve prey capture, delivery to nestlings, and reproductive success for Spotted Owls in southern California
<p>Predator-prey interactions can be profoundly influenced by vegetation conditions, particularly when predator and prey prefer different habitats. Although such interactions have proven challenging to study for small and cryptic predators, recent methodological advances substantially improve opportunities for understanding how vegetation influences prey acquisition and strengthen conservation planning for this group. The California Spotted Owl (<em>Strix</em> <em>occidentalis</em> <em>occidentalis</em>) is well-known as an old-forest species of conservation concern, but whose primary prey in many regions – woodrats (<em>Neotoma</em> spp.) – occurs in a broad range of vegetation conditions. Here, we used high-resolution GPS tracking coupled with nest video monitoring to test the hypothesis that prey capture rates vary as a function of vegetation structure and heterogeneity, with emergent, reproductive consequences for Spotted Owls in Southern California. Foraging owls were more successful capturing prey, including woodrats, in taller multilayered forests, in areas with higher heterogeneity in vegetation types, and near forest-chaparral edges. Consistent with these findings, Spotted Owls delivered prey items more frequently to nests in territories with greater heterogeneity in vegetation types and delivered prey biomass at a higher rate in territories with more forest-chaparral edge. Spotted Owls had higher reproductive success in territories with higher mean canopy cover, taller trees, and more shrubby vegetation. Collectively, our results provide additional and compelling evidence that a mosaic of large tree forests with complex canopy and shrubby vegetation increases access to prey with potential reproductive benefits to Spotted Owls in landscapes where woodrats are a primary prey item. We suggest that forest management activities that enhance forest structure and vegetation heterogeneity could help curb declining Spotted Owl populations while promoting resilient ecosystems in some regions.</p>
Io hot spots map derived by Juno/JIRAM orbits: 10, 11, 16, 17, 18, 20, 24, 25, 26, 27, 32, 33
<p>Io hot spots map GIS shapefile derived by Juno/JIRAM orbits: 10, 11, 16, 17, 18, 20, 24, 25, 26, 27, 32, 33</p>
Text-fig. 6. Taimyria triassica NAUGOLNYKH et MOGUTCHEVA gen. et sp. nov., holotype 4287/6. Epidermal-cuticular structure of upper surface of seed-bearing capsule. a–c, e–g: cuticles of upper surface of seed-bearing capsule, b – detail of (a), notice small white spot at picture center, which could be interpreted as scar of small monocellular trichome; d: conducting strand going to seed scar. Locality: Tsvetkov Cape; Lower Triassic, Induan; Keshin Formation. Scale bar 200 µm (a, c, d, g), 100 µm (e, f). in Taimyria Gen. Nov., A New Genus Of Evolutionary Advanced Gymnosperms From Triassic Of The Taimyr Peninsula, Siberia, Russia
Text-fig. 6. Taimyria triassica NAUGOLNYKH et MOGUTCHEVA gen. et sp. nov., holotype 4287/6. Epidermal-cuticular structure of upper surface of seed-bearing capsule. a–c, e–g: cuticles of upper surface of seed-bearing capsule, b – detail of (a), notice small white spot at picture center, which could be interpreted as scar of small monocellular trichome; d: conducting strand going to seed scar. Locality: Tsvetkov Cape; Lower Triassic, Induan; Keshin Formation. Scale bar 200 µm (a, c, d, g), 100 µm (e, f).
Keyword Spotting with African Languages
<p><strong>Keyword spotting refers to the task of learning to detect spoken keywords. It interfaces all modern voice-based virtual assistants on the market: Amazon’s Alexa, Apple’s Siri, and the Google Home device. Contrarily to speech recognition models, keyword spotting doesn’t run on the cloud, but directly on the device. </strong></p> <p><strong>The motivation of this paper is to extend the Speech commands dataset (Warden 2018) with African languages. In particular, we are going to focus on 6 Senegalese languages: Wolof, Pulaar, Serer, Mandinka, Diola, Soninke. </strong></p> <p><strong>The choice of these languages is guided, on the one hand, by their status as languages considered to be the languages of the first generation, that is to say, the first codified languages (endowed with a writing system and considered by the state of Senegal as national languages) with decree n ° 68-871 of July 24, 1968. On the other hand, they represent the languages that are most spoken in Senegal.</strong></p>
Data and code from: Three decades of wildlife-vehicle collisions in a protected area: main roads and long-distance commuting trips to migratory prey increase spotted hyena roadkills in the Serengeti
<p>This is the first release. Potential updates will be available on GitHub: <a href="https://github.com/MarwanNaciri/Three_decades_of_spotted_hyena_roadkill_in_a_protected_area">https://github.com/MarwanNaciri/Three_decades_of_spotted_hyena_roadkill_in_a_protected_area</a></p>
Fig. 19 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 19. Lacronia tenuis (Roewer, 1917) comb. nov., ♂ (MNRJ 260). A. Habitus, dorsal view. B. Ocularium, frontal view. C. Armature of mesotergum area III, posterior view. D. Habitus, lateral view. E. Left Fe–Ti III, proventral view. F. Right Fe–Ti IV, dorsal view. G. Same, prolateral view. H. Same, ventral view. I. Same, retro-lateral view. J. Right Mt–Ta IV, retro-lateral view. Scale bars: A, D–J = 3 mm; B–C = 1 mm.
Fig. 14 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 14. South America, showing the distribution of the Lacronia nigra (B. Soares, 1942) comb. nov. non-type specimens (as white circles). The legend refers to the type localities of Discocyrtus niger B. Soares, 1942 (Piraí) and Discocyrtus rarus B. Soares, 1944 (Alto da Serra). The area shaded in magenta represents Chile, the type locality of Discocyrtus fazi Piza, 1942.
Fig. 15. Lacronia ricardoi Kury, 2003 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 15. Lacronia ricardoi Kury, 2003 (MZSP 21373), specimens in alcohol. A–C. Holotype, ♂ (MZSP 21373). A. Habitus, dorsal view. B. Same, lateral view. C. Same, ventral view. D–F. Paratype, ♀ (MZSP 10589). D. Habitus, dorsal view. E. Same, lateral view. F. Same, ventral view. Scale bars = 1 mm.
Fig. 18 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 18. Lacronia serripes (Mello-Leitão, 1923), ♂ (MNRJ 9973), penis, distal part. A. Dorsal view. B. Right lateral view. C. Ventral view. D. Left lateral view. Scale bars = 100 μm.
Fig. 13 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 13. Lacronia nigra (B. Soares, 1942) comb. nov., ♂ (MNRJ 9207ꜝ), penis, distal part. A. Dorsal view. B. Lateral view. C. Ventral view. Scale bars = 20 μm.
Fig. 10. Lacronia spp. A. L. camboriu Kury, 2003 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 10. Lacronia spp. A. L. camboriu Kury, 2003, ♂, holotype (MNRJ 4956ꜝ), specimen in alcohol, from Brazil, Santa Catarina, Balneário Camboriú. B. L. ceci Kury & Orrico, 2006, ♂, specimen in vivo, from Brazil, Rio de Janeiro, Teresópolis. Photographs by Adriano Kury (A) and Glauco Machado (B).
Fig. 9 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 9. Lacronia spp., female specimens, dorsal habitus. A. L. boraceae (B. Soares, 1942) comb. nov., holotype (MZSP 114ꜝ), schematic illustration. B. L. nigra (Mello-Leitão, 1923) comb. nov., holotype of Discocyrtus fazi Piza, 1942 (MZSP 1549ꜝ), schematic illustration. C. L. serripes Mello-Leitão, 1923 (MZSP 9973). Scale bars = 3 mm.
Fig. 11 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 11. Lacronia ceci Kury & Orrico, 2006, ♂ (MNRJ 6945ꜝ), penis, distal part. A. Dorsal view. B. Lateral view. C. Ventral view. D. Detail of stylus and ventral process, latero-dorsal view. Scale bars: A–C = 50 μm; D = 20 μm.
Fig. 8 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 8. Lacronia boraceae (B. Soares, 1942) comb. nov., ♂ (MNRJ-HS 122ꜝ), penis, distal part. A. Dorsal view. B. Lateral view. C. Ventral view. D. Detail of stylus and ventral process apex, dorsal view. Scale bars: A = 50 μm; B–C = 100 μm; D = 10 μm.
Fig. 6 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 6. Lacronia boraceae (B. Soares, 1942) comb. nov., ♂ (MNRJ-HS 122ꜝ), specimen in alcohol. A. Habitus, dorsal view. B. Same, ventral view. C. Same, lateral view. D. Armature of mesotergum area III, free tergites I–III and anal operculum, posterior view. E. Right Pa–Ti IV, retro-lateral view. Scale bars = 1 mm.
Fig. 7 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 7. Lacronia boraceae (B. Soares, 1942) comb. nov., ♂ (MNRJ-HS 122ꜝ). A. Habitus, dorsal view. B. Ocularium, frontal view. C. Armature of mesotergum area III, posterior view. D. Right Fe III, prodorsal view. E. Habitus, lateral view. F. Left Fe IV, proventral view. G. Right Fe IV, retro-ventral view. H. Right Pa–Ti IV, proventral view. I. Right Pa–Ti IV, ventral view. Scale bars: A, E = 4 mm; B–C = 1 mm; D, H–I = 2 mm; F–G = 3 mm.
Fig. 5 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 5. Southeasten and Southern regions of Brazil, showing the distribution of the Lacronia spp. The area shaded in green represents the Atlantic province, as proposed by Morrone et al. (2022).
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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.