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1,568 results for “slope”
Testing paleomagnetic dating accuracy on pre-historic flank eruptions from SE slope of Etna volcano
<p>Paleomagnetic and petrographic data used for supporting the work of Magli et al. (Testing paleomagnetic dating accuracy on pre-historic flank eruptions from SE slope of Etna volcano):</p><ul><li>"AF_Demag.xlsx" = Alternating Field (AF) demagnetization data obtained at the Laboratory of Paleomagnetism (INGV of Rome) for each demagnetization step (20 up to 120 mT) for all samples.</li><li>"Bulk_susceptibility_&_Q.xlsx" = NRM (Natural Remanent Magnetization), k (susceptibility), J (induced magnetization intensity) and Q (Königsberger ratio, NRM/J) values obtained for each sample.</li><li>"ImageJ_analyses.xlsx" = abundance values (volume %) of vesicles and mineralogical phases obtained by ImageJ software (along with phenocrysts dimensions) for each random photo, for each sampling site and for each lava flow studied.</li><li>"Therm_curve.xlsx" = Susceptibility and temperature values obtained thorugh the MFK1 Kappabridge to provide thermomagnetic curves.</li></ul>
Data for publication "On the flow behaviour of unconfined dual porosity aquifers with sloping base"
<p>Data used in the paper </p> <p>"On the flow behaviour of unconfined dual porosity aquifers with sloping base", </p> <p>by Konstantinos N. Moutsopoulos, John N. E. Papaspyros, Antonis D. Koussis, Frédérick Delay, and Marwan Fahs, </p> <p>submitted to Advances in Water Research.</p>
Diablo model output for LES basal slope effects study
Open the record for dataset details and reuse information.
Data for "Tracking the nearfield evolution of an initially shallow, neutrally-buoyant plane jet over a sloping bottom boundary"
<p>This folder contains all the data set for figures in the paper titled as "Tracking the nearfield evolution of an initially shallow, neutrally-buoyant plane jet over a sloping bottom boundary". </p>
Importance of ice elasticity in simulating tide-induced grounding line variations along prograde bed slopes
<p>Maslennikova_data.zip contains the Differential Interferometric Synthetic Aperture Radar (DInSAR) interferograms and the manually mapped grounding lines utilized for short-term tide-induced grounding line migrations analysis.</p>
Lunar PSR catalog: Area, Length, Slope, H/L ratio
<p>Catalog of lunar northern and southern PSRs with length, area, H/L ratio, and slope measurements. </p>
FIGURE 5 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 5. Terrestrial habitats and hosts plants of Athis hechtiae and A. miastagma (Castniidae). A) Xeric shrubland of the Tehuacán Valley Matorral eco-region, Tehuacán-Cuicatlán Valley, Puebla, typical habitat of A. hechtiae; B) Hechtia tehuacana (Bromeliaceae), host of A. hechtiae; C) Hechtia santanae, host of A. miastagma; D) Tropical deciduous forests, with a multilayered structure, Tuxcacuesco, Jalisco, typical habitat of A. miastagma.
FIGURE 4 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 4. Maximum Likelihood phylogeny of some Castniidae species based on COI barcoding sequences. Numbers at each node represent support values according to 1000 ultrafast bootstrap replicates as implemented in IQ-TREE. Note: Photographs have been size-adjusted only for illustrations purposes. List of taxa with accession numbers is given on Table 1.
FIGURE 3 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 3. Average genetic distances (y-axes) of intraspecific A. hechtiae, genetic distances of A. miastagma to A. hechtiae, and intraspecific A. miastagma.
FIGURE 2 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 2. Male genitalia of Athis hechtiae (left) from the Tehuacán-Cuicatlán Valley (C, drawing by Simeão Moraes) and A. miastagma (right) from D, Jalisco; E, F, Guerrero (The latter based on the holotype genitalia). Each set shows the genital armature (top) and aedeagus (bottom).
FIGURE 6 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 6. Maps of a section of Mexico showing known collecting localities for Athis hechtiae (blue circles) (Tehuacán-Cuicatlán Valley) and Athis miastagma (blue squares) (mainly in the Balsas Basin, flowing through the Sierra Madre del Sur and into the Pacific, limited in the northwest by the western mountainous section of the Trans-Mexican Volcanic Belt; to the East it does not enter the Tehuacán Valley, and to the Southeast does not cross the Mixtec region). The red square indicates only the presence of A. miastagma in Michoacán. It is located in the center of the state because the supposed collecting locality (Putja) could not be identified. The red circles are doubtful localities of occurrence of A. hechtiae in Presidio, Veracruz, and Totolapán, Oaxaca. Top figure is an ecoregion map based on Dinerstein et al. (2017); the bottom one is a hypsographic map. (Maps: Bolívar Garcete)
FIGURE 1 in Reinstatement of Athis miastagma (Dyar, 1925) (Lepidoptera: Castniidae) as a valid species inhabiting the Pacific slope of Central Mexico
FIGURE 1. Males (top row) and females (bottom row) of Athis hechtiae (left) and A. miastagma (right), from Mexico.
Distribution. Known from the southern slopes of Himalayas in N India (including Sikkim), Nepal, and Bhutan. in Moschidae
Distribution. Known from the southern slopes of Himalayas in N India (including Sikkim), Nepal, and Bhutan.
Distribution. The range is unknown, but it is believed to occur on the W slopes and foothills of the Andes of W Colombia, in the region of Quindio and Riseralda. in Aotidae
Distribution. The range is unknown, but it is believed to occur on the W slopes and foothills of the Andes of W Colombia, in the region of Quindio and Riseralda.
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department). in Atelidae
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department).
Subspecies and Distribution. A. h. hybridus 1. Geoffroy Saint-Hilaire, 1829 — N Colombia (from the right bank of the Rio Magdalena, N to the S slopes of the Sierra Nevada de Santa Marta and the N of the Serrania de Perija, and in the middle Rio Magdalena Valley at least to the departments of Caldas and Cundinamarca; two populations on the slopes of the Cordillera Oriental on the Venezuelan border (one in the Rio Catatumbo watershed in the Norte de Santander Department and the other in the NE piedmont forest in Arauca Department) and N & NW Venezuela (along the SE part of the Cordillera de la Costa in the states of Miranda and probably Vargas, and on both sides of the Venezuelan Andesin the states of Zulia, Tachira, Mérida, Trujillo, Portuguesa, Apure, and Barinas, in the E in the piedmont and lowland forests of San Camilo and Ticoporo, and in the Win the piedmont forest around S Lake Maracaibo to the Sierra de Perija). A. h. brunneus Gray, 1871 — N Colombia in the departments of Antioquia, Bolivar, and Caldas, between the lower rios Cauca and Magdalena. in Atelidae
Subspecies and Distribution. A. h. hybridus 1. Geoffroy Saint-Hilaire, 1829 — N Colombia (from the right bank of the Rio Magdalena, N to the S slopes of the Sierra Nevada de Santa Marta and the N of the Serrania de Perija, and in the middle Rio Magdalena Valley at least to the departments of Caldas and Cundinamarca; two populations on the slopes of the Cordillera Oriental on the Venezuelan border (one in the Rio Catatumbo watershed in the Norte de Santander Department and the other in the NE piedmont forest in Arauca Department) and N & NW Venezuela (along the SE part of the Cordillera de la Costa in the states of Miranda and probably Vargas, and on both sides of the Venezuelan Andesin the states of Zulia, Tachira, Mérida, Trujillo, Portuguesa, Apure, and Barinas, in the E in the piedmont and lowland forests of San Camilo and Ticoporo, and in the Win the piedmont forest around S Lake Maracaibo to the Sierra de Perija). A. h. brunneus Gray, 1871 — N Colombia in the departments of Antioquia, Bolivar, and Caldas, between the lower rios Cauca and Magdalena.
FIGURE 2 in Two new species of Monstera (Araceae: Monsteroideae) from the Pacific slope of the Andes in Colombia
FIGURE 2. Distribution map for Monstera momoi. (circles) and Monstera kikiae. (triangles). National Natural Parks are shown in green from top to bottom Las Orquídeas, Tatamá and Farallones de Cali.
FIGURE 3 in Two new species of Monstera (Araceae: Monsteroideae) from the Pacific slope of the Andes in Colombia
FIGURE 3. Comparison of Monstera momoi, Monstera kikiae and similar species. A-B, Monstera momoi. C-D, M. dissecta. E-F, M. kikiae. G-H, M. oreophila. A, Leaf blade. B, Petiole apex showing the sheath and geniculum. C, Petiole apex showing the sheath and geniculum. D, Leaf blade. E, Leaf blade. F, Inflorescence in post-anthesis. G, Inflorescence in anthesis. H, Leaf blade. Photographs A-D by Marco Cedeño; F-H by Alejandro Zuluaga.
FIGURE 4 in Two new species of Monstera (Araceae: Monsteroideae) from the Pacific slope of the Andes in Colombia
FIGURE 4. Monstera momoi sp. nov. A, Undeveloped inflorescence. B, Partially-opened inflorescence, frontal view. C, Part-opened inflorescence, dorsal view. D, Infructescence. E, Fertile flower in lateral view (left) and in longitudinal section (right). F, Sterile flower in lateral view (left) and in longitudinal section (right). G, Adult plant. H, Stylar cap, dorsal view (left), and individual stamen (right). Photographs by Marco Cedeño.
F in Biology and life cycle of Scopelocheirus hopei (A. Costa, 1851), a scavenging amphipod from the continental slope of the Mediterranean
F. 4. Sexual development. Male: (A) calceoli on the antennae 2. Female: (B) St.1 without any oostegites; (C) St.2 with rudimentary oostegite; (D) St.3 oostegite developing; (E) the 'buds', place of the future setae, at the extremity of the oostegite; (F) St.4 with a developed oostegite, note its length relative to the other stages; (G) extremity of St.4 oostegite showing the insertion points of the setae; (H) St.5 the extremity of the oostegite bearing setae.
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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.