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1,473 results for “Geographic distribution”
Figure 2 in How can global climate change influence the geographic distribution of the eucalyptus yellow beetle? Modeling and prediction for Brazil
Figure 2. Predicting of potential areas to the occurrence of Costalimaita ferruginea in the period of 2041-2060, in two climate change scenarios, Representative Concentration Pathways (RCP) 4.5 e 8.5 (W/m2), using the algorithm Envelope Score (AUC = 0.808). The numbers 1 to 5 represent the Brazilian biomes, being 1 = Amazônia, 2 = Caatinga, 3 = Cerrado, 4 = Pantanal, 5 = Mata Atlântica e 6 = Pampa.
Figures 14–17 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figures 14–17: Rhopalurus pintoi kourouensis ssp. n. 14. Carapace. 15. Metasoma and telson, lateral aspect. 16–17. Metasoma and telson, dorsal and ventral aspects.
Figures 10–13 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figures 10–13: Rhopalurus pintoi kourouensis ssp. n. 10. Chela, dorso-external aspect, showing trichobothria and very intense setation. 11. Chela, idem, represented without setation. 12–13. Patella and femur, dorsal aspect. Again an important setation can be observed.
Figures 5–9 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figures 5–9: Rhopalurus crassicauda paruensis ssp. n., male holotype. 5–7. Chela, dorso-external, ventral and internal aspects, showing trichobothria. 8–9. Tarsi of leg IV, lateral and ventral aspects, showing setation.
Figure 4 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figure 4: Present distribution of savannah formations in South America (after Sarmiento, 1984). Arrows indicated distinct savannah fragments inhabited by Rhopalurus species. 1. Llanos of the Magdalena (R. caribensis); 2. Llanos of Orinoco (R. laticauda); 3. Savannahs of the Rio Branco-Rupununi (R. pintoi & R. crassicauda); 4. Campos de Paru (R. crassicauda paruensis ssp. n.); 5. Coastal savannahs of the Guayanas (R. pintoi kourouensis ssp. n.).
Figure 1 in The geographic pattern of distribution of the genus Rhopalurus Thorell, 1876 in the Guayana-Amazon region (Scorpiones: Buthidae)
Figure 1: Presumed dispersal tracks of Rhopalurus spp., between 18,000 and 13,000 years BP. A and B illustrate possible corridors between North-South and East-West savannah formations which coalesced during past dry periods (base map after Ab'Saber, 1977).
Fig. 1 in Maximum entropy niche-based modeling (Maxent) of potential geographical distribution of Coreura albicosta (Lepidoptera: Erebidae: Ctenuchina) in Mexico
Fig. 1. Model of potential distribution of Coreura albicosta with enhancement of the favorable climatic regions for this species, and superposition with the network of protected areas of México. Gray: lower probability of appropriate environmental conditions for distribution of the species. Light gray sections represent the decision threshold (0.2426) in which the grids are favorable for the distribution of the species. Darker sections inside light gray: areas with high probability of presence of the species. Black dots indicate the known distribution of the species. The protected areas are represented with a black line.
Fig. 2 in Prevalence and geographical distribution of amphistomes of African wild ruminants: A scoping review
Fig. 2. Map showing geographical distribution of amphistomes in wild ruminants in Africa (1900–2022).
Fig. 1 in Geographic Distribution and Genetic Structures of the Tideland Snails and in Taiwan and Japan.
Fig. 1. Sampling sites of Pirenella nipponica and P. asiatica. Sampling at Japanese sites was carried out in the previous study (Kojima et al. 2006). Areas shown in the pie graphs reflect the number of collected individuals. Black and white sectors in the pie graphs indicate relative frequencies of P. nipponica and P. asiatica.
Fig. 2. A in Geographic Distribution and Genetic Structures of the Tideland Snails and in Taiwan and Japan.
Fig. 2. A statistical parsimony haplotype network of Pirenella nipponica (a) and P. asiatica (b) based on nucleotide sequences of the mitochondrial cytochrome c oxidase subunit I (COI) gene. The areas of the circles are proportional to the frequency of the occurrence of the haplotypes. Numbers of haplotypes are same as those in table 2 and Kojima et al. (2006). Colors of sections denote the relative occurrence frequency of individuals collected in each area. The haplotypes that were not detected in the sample are indicated by small black circles.
Fig. 1 in Toxocariasis in Carnivora from Argentinean Patagonia: Species molecular identification, hosts, and geographical distribution
Fig. 1. Collection sites of specimens of Felidae, Mustelidae, and Canidae in Lanín and Nahuel Huapi National Parks from Argentinean Patagonia.
gellum black. Femora all black or forefemur ferruginous in apicoventral half; foretibia brown or ferruginous, midtibia brown ferruginous, hindtibia brown; tarsi varying from brown to ferruginous. ♂.– Unknown. GEOGRAPHIC DISTRIBUTION.– Known only from higher elevations (1020-1130 m above sea level) of Ranomafana National Park, Madagascar. RECORDS (Fig. 29).— All specimens were collected in Ranomafana National Park, Fianarantsoa Province. Holotype: ♀, Belle Vue at Talatakely at 21º15.99'S 47º25.21'E, alt. 1020 m, 14-21 Jan 2002, M. Irwin and R. Harin 'Hala (CAS). Paratypes: Radio tower at forest edge at 21º15.05'S 47º24.43'E, alt. 1130 m, 23 Aug – 7 Sept 2006 and 1-11 Nov 2006, M. Irwin and R. Harin 'Hala (2 ♀, CAS); same data as holotype except 22-28 Nov 2001 and R. Harin 'Hala alone (1 ♀, CAS); Vohiparara at 21º13.57'S 47º22.19'E, alt. 1110 m, 22-28 Nov 2001, R. Harin 'Hala (1 ♀, CAS). FIGURE 29. Collecting localities of Tachytes melanogaster sp. nov. in A Review of the Wasp Genus Tachytes Panzer, 1806 of Madagascar (Hymenoptera: Crabronidae)
gellum black. Femora all black or forefemur ferruginous in apicoventral half; foretibia brown or ferruginous, midtibia brown ferruginous, hindtibia brown; tarsi varying from brown to ferruginous. ♂.– Unknown. GEOGRAPHIC DISTRIBUTION.– Known only from higher elevations (1020-1130 m above sea level) of Ranomafana National Park, Madagascar. RECORDS (Fig. 29).— All specimens were collected in Ranomafana National Park, Fianarantsoa Province. Holotype: ♀, Belle Vue at Talatakely at 21º15.99'S 47º25.21'E, alt. 1020 m, 14-21 Jan 2002, M. Irwin and R. Harin 'Hala (CAS). Paratypes: Radio tower at forest edge at 21º15.05'S 47º24.43'E, alt. 1130 m, 23 Aug – 7 Sept 2006 and 1-11 Nov 2006, M. Irwin and R. Harin 'Hala (2 ♀, CAS); same data as holotype except 22-28 Nov 2001 and R. Harin 'Hala alone (1 ♀, CAS); Vohiparara at 21º13.57'S 47º22.19'E, alt. 1110 m, 22-28 Nov 2001, R. Harin 'Hala (1 ♀, CAS). FIGURE 29. Collecting localities of Tachytes melanogaster sp. nov.
Success in Mobile and Ubiquitous Learning: Indicators of Effectiveness-Figure 1. Geographical distribution of the case studies
<p>The 50 cases of mobile and ubiquitous learning practices covered 14 countries/regions, including China, Japan, Taiwan, Korea, Sri Lanka, Turkey, Spain, Greece, the Netherlands, Britain, Australia, New Zealand, South Africa and the USA. Figure 1 shows the geographical distribution of the cases. Among the 50 cases, 70% were conducted in Asia, 16% in Europe, 4% in Oceania, 4% in Africa, and 2% in North America. Therefore, the results of this study represent more of the situation in Asia.</p>
Figure 1 in New records, extended and updated geographic distribution of the South American native antlion Dimares elegans (Perty, 1833) (Neuroptera, Myrmeleontidae)
Figure 1 Dimares elegans (Perty, 1833) (GEEFAA/UFRN-1342), female specimen collected in Quintos de Cima, Equador, Rio Grande do Norte, Brazil. (a) General dorsal view, (b) dorsal view of the apex of the posterior wing, (c) anterior legs, (d) posterior legs.
Figure 3 in New records, extended and updated geographic distribution of the South American native antlion Dimares elegans (Perty, 1833) (Neuroptera, Myrmeleontidae)
Figure 3 Sampling site and observation records of the antlion Dimares elegans (Perty, 1833) in the new easternmost records, Rio Grande do Norte, Brazil. (a) Sítio Trapiá, Quintos de Cima, sampling site of the specimen GEEFAA/UFRN-1342, (b) photographic record on previously mentioned locality, (c) photographic record on Mossoró (kindly provided by Heinz T Dantas-UERN).
Figure 2 in New records, extended and updated geographic distribution of the South American native antlion Dimares elegans (Perty, 1833) (Neuroptera, Myrmeleontidae)
Figure 2 Updated geographic distribution of the antlion Dimares elegans (Perty, 1833) highlighting primary and secondary data according to bioregionalization of terrestrial ecosystems.
Figure 5 in The taxonomic status and geographic distribution of the European hare (Lepus europaeus Pallas, 1778) in Turkey (Mammalia: Lagomorpha)
Figure 5. The group centroids obtained from discriminant functions: 1 = Thracian specimen, 2 = Southwest Anatolian population, 3 = Central and East-Central Anatolian population, 4 = Northeast Anatolian population, 5 = Southeast Anatolian population.
Text-fig. 1. Bohemian Massif with position of the Prague Basin (in black) and distribution of Ordovician rocks in the Prague Basin, with geographic position of main localities of the siliceous nodules. in Porambonites Havliceki Sp. Nov., A New Brachiopod From The Šárka Formation (Darriwilian) From Bohemia And Its Contribution To Early History Of The Porambonitidae
Text-fig. 1. Bohemian Massif with position of the Prague Basin (in black) and distribution of Ordovician rocks in the Prague Basin, with geographic position of main localities of the siliceous nodules.
Figure 57-64. Gastrosericus wroughtoni Cameron. 57-58, female. 57 in On the geographic distribution of Gastrosericus Spinola, 1839 (Hymenoptera: Crabronidae) in India
Figure 57-64. Gastrosericus wroughtoni Cameron. 57-58, female. 57, Gaster; 58, Pygidium; 59-64, male. 59, Habitus, lateral view; 60, Habitus, dorsal view; 61, Head, dorsal view; 62, Clypeus; 63, Propodeum, dorsal view; 64, Antennae.
Figure 49-56. Gastrosericus wroughtoni Cameron, female. 49 in On the geographic distribution of Gastrosericus Spinola, 1839 (Hymenoptera: Crabronidae) in India
Figure 49-56. Gastrosericus wroughtoni Cameron, female. 49, Habitus, lateral view; 50, Habitus, dorsal view; 51, Head, frontal view; 52, Clypesus; 53, Head & thorax; 54, Propodeum, dorsal view; 55, Antennae; 56, Forewing.
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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.