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6,783 results for “orientator”
Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - twig - orientation of petioles
Image of Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - twig - orientation of petioles
Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - leaf - showing orientation on twig
Image of Hibiscus moscheutos ssp. lasiocarpos (Malvaceae) - leaf - showing orientation on twig
Euonymus atropurpureus (Celastraceae) - twig - orientation of petioles
Image of Euonymus atropurpureus (Celastraceae) - twig - orientation of petioles
Campsis radicans (Bignoniaceae) - twig - orientation of petioles
Image of Campsis radicans (Bignoniaceae) - twig - orientation of petioles
Rejilla 2013-2023 de datos diarios de precipitación total, temperatura a 2 m, presión a 2 m del centro-oriente de Cuba
<p>Rejilla 2013-2023 de datos diarios de precipitación total, temperatura a 2 m, presión a 2 m del centro-oriente de Cuba generada con el WRF v4, forzado con ERA5. Postprocesado a datos diarios en superficie de variables meteorológicas.</p>
Supply Chain 5.0: technology-based and resilience-oriented framework - datasets
Open the record for dataset details and reuse information.
Confocal images from: Cell density, alignment, and orientation correlate with C-signal-dependent gene expression during Myxococcus xanthus development
<p>Starving <em>Myxococcus xanthus</em> bacteria use short-range C-signaling to coordinate their movements and construct multicellular mounds, which mature into fruiting bodies as rods differentiate into spherical spores. Differentiation requires efficient C-signaling to drive the expression of developmental genes, but how the arrangement of cells within nascent fruiting bodies (NFBs) affects C-signaling is not fully understood. Here, we used confocal microscopy and cell segmentation to visualize and quantify the arrangement, morphology, and gene expression of cells near the bottom of NFBs at much higher resolution than previously achieved. We discovered that "transitioning cells" (TCs), intermediate in morphology between rods and spores, comprised 10 to 15% of the total population. Spores appeared midway between the center and the edge of NFBs early in their development and near the center as maturation progressed. The developmental pattern as well as C-signal-dependent gene expression in TCs and spores were correlated with cell density, the alignment of neighboring rods, and the tangential orientation of rods early in the development of NFBs. These dynamic radial patterns support a model in which the arrangement of cells within the NFBs affects C-signaling efficiency to regulate precisely the expression of developmental genes and cellular differentiation in space and time. Developmental patterns in other bacterial biofilms may likewise rely on short-range signaling to communicate multiple aspects of cellular arrangement, analogous to juxtacrine and paracrine signaling during animal development.</p>
FIGURES 78–90 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 78–90. Eurhadina (Singhardina) immatura sp. nov. 78, habitus, dorsal view. 79, habitus, lateral view. 80, head and thorax, dorsal view. 81, face. 82, male pygofer side, lateral view. 83, hind part of pygofer, lateral view. 84, subgenital plate, connective, paramere and sternite IX, dorsal view. 85, apex of subgenital plate, dorsal view. 86, connective, dorsal view. 87, paramere, dorsal view. 88, aedeagus, posterior view. 89, apex of aedeagal shaft, dorsal view. 90, aedeagus, lateral view.
FIGURES 52–64 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 52–64. Eurhadina (Singhardina) fumosa sp. nov. 52, habitus, dorsal view. 53, habitus, lateral view. 54, head and thorax, dorsal view. 55, face. 56, male pygofer side, lateral view. 57, hind part of pygofer, lateral view. 58, paramere, connective, subgenital plate and sternite IX, dorsal view. 59, apex of subgenital plate, dorsal view. 60, connective, dorsal view. 61, paramere, dorsal view. 62, aedeagus, posterior view. 63, apex of aedeagal shaft, dorsal view. 64, aedeagus, lateral view.
FIGURES 26–38 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 26–38. Eurhadina (Singhardina) dissimilis sp. nov. 26, habitus, dorsal view. 27, habitus, lateral view. 28, head and thorax, dorsal view. 29, face. 30, male pygofer side, lateral view. 31, hind part of pygofer, lateral view. 32, subgenital plate, connective, paramere and sternite IX, dorsal view. 33, apex of subgenital plate, dorsal view. 34, connective, dorsal view. 35, paramere, dorsal view. 36, aedeagus, posterior view. 37, apex of aedeagal shaft, dorsal view. 38, aedeagus, lateral view.
FIGURES 39–51 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 39–51. Eurhadina (Singhardina) flatilis sp. nov. 39, habitus, dorsal view. 40, habitus, lateral view. 41, head and thorax, dorsal view. 42, face. 43, male pygofer side, lateral view. 44, hind part of pygofer, lateral view. 45, paramere, connective, subgenital plate and sternite IX, dorsal view. 46, apex of subgenital plate, dorsal view. 47, connective, dorsal view. 48, paramere, dorsal view. 49, aedeagus, posterior view. 50, apex of aedeagal shaft, dorsal view. 51, aedeagus, lateral view.
FIGURES 14–25 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 14–25. Eurhadina (Singhardina) pookiewica rec. nov. 14, habitus, dorsal view. 15, habitus, lateral view. 16, head and thorax, dorsal view. 17, face. 18, male pygofer side, lateral view. 19, hind part of pygofer, lateral view. 20, subgenital plate, connective and paramere, dorsal view. 21, apex of subgenital plate, dorsal view. 22, connective, dorsal view. 23, aedeagus, posterior view. 24, apex of aedeagal shaft, dorsal view. 25, aedeagus, lateral view.
FIGURES 1–13 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 1–13. Eurhadina (Singhardina) krispinilla rec. nov. 1, habitus, dorsal view. 2, habitus, lateral view. 3, head and thorax, dorsal view. 4, face. 5, male pygofer side, lateral view. 6, hind part of pygofer, lateral view. 7, subgenital plate, connective, paramere and sternite IX, dorsal view. 8, apex of subgenital plate, dorsal view. 9, connective, dorsal view. 10, paramere, dorsal view. 11, aedeagus, posterior view. 12, apex of aedeagal shaft, dorsal view. 13, aedeagus, lateral view.
FIGURES 65–77 in First records of the Oriental Eurhadina (Singhardina) robusta species group from China with descriptions of five new species (Hemiptera: Cicadellidae: Typhlocybinae)
FIGURES 65–77. Eurhadina (Singhardina) furca sp. nov. 65, habitus, dorsal view. 66, habitus, lateral view. 67, head and thorax, dorsal view. 68, face. 69, male pygofer side, lateral view. 70, hind part of pygofer, lateral view. 71, paramere, connective and subgenital plate, dorsal view. 72, apex of subgenital plate, dorsal view. 73, connective, dorsal view. 74, paramere, dorsal view. 75, aedeagus, posterior view. 76, apex of aedeagal shaft, dorsal view. 77, aedeagus, lateral view.
Distribution. Amazonian Brazil, S of the Rio Amazonas-Solimoes, W of the rios Tapajos-Teles Pires to the Rio Ucayali in NE Peru (where it is replaced by A. belzebuth on the left bank of the lower Ucayali); it crosses the middle Ucayali S of the Rio Cushabatay (a left bank tributary of the Ucayali), extending to the interfluvium of the rios Ucayali and Huallaga, then S along the Cordillera Oriental, and into N & C Bolivia S to ¢.17° S, and from there, NE through Noel Kempff Mercado National Park. in Atelidae
Distribution. Amazonian Brazil, S of the Rio Amazonas-Solimoes, W of the rios Tapajos-Teles Pires to the Rio Ucayali in NE Peru (where it is replaced by A. belzebuth on the left bank of the lower Ucayali); it crosses the middle Ucayali S of the Rio Cushabatay (a left bank tributary of the Ucayali), extending to the interfluvium of the rios Ucayali and Huallaga, then S along the Cordillera Oriental, and into N & C Bolivia S to ¢.17° S, and from there, NE through Noel Kempff Mercado National Park.
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela. in Atelidae
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela.
Distribution. Endemic to Trinidad I and Venezuela E of Lake Maracaibo, along the coast from Falcon State to Miranda State, the northern Mts (Cordillera Oriental, Cordillera Central, and Coro System), and extending S through the Llanos to the Rio Orinoco; it may extend into Arauca State, Colombia. in Atelidae
Distribution. Endemic to Trinidad I and Venezuela E of Lake Maracaibo, along the coast from Falcon State to Miranda State, the northern Mts (Cordillera Oriental, Cordillera Central, and Coro System), and extending S through the Llanos to the Rio Orinoco; it may extend into Arauca State, Colombia.
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.
Distribution. Not well known, but includes S Venezuela (upper Orinoco Basin, limited by the Llanos/forest interface to the W and by the left bank of the Rio Caura in the E), NW Brazil (N of the Rio Solimoes as far as the mouth of the Rio Japura, E to the Rio Negro, throughout the region N of the Rio Negro and W of the Rio Branco in Amazonas and Roraimastates), E Colombia (in the piedmont of the Cordillera Oriental as far N as the Rio Upia drainage in Boyaca Department, including the region of Sierra de la Macarena, E Meta Department, and S to the Coehmani rapids of the Rio Caqueta in the SE of Caqueta Department; it is rare W of the Rio Yari and has been seen on the upper Rio Mesay, opposite the mouth of the Rio Pira-Parana on the right bank of the Rio Apaporis, and the lower right bank of the Apaporis), E Ecuador and NE Peru (restricted to the S of the Rio Napo, extending into N Peru between the rios Putumayo and Amazonas, along the left bank of the Rio Ucayali, and including the basins of the rios Napo, Tigre, Maranén, Pastaza, Pacaya, and Samiria, S as far as the Rio Cushabatay, a tributary of the Rio Ucayali). in Atelidae
Distribution. Not well known, but includes S Venezuela (upper Orinoco Basin, limited by the Llanos/forest interface to the W and by the left bank of the Rio Caura in the E), NW Brazil (N of the Rio Solimoes as far as the mouth of the Rio Japura, E to the Rio Negro, throughout the region N of the Rio Negro and W of the Rio Branco in Amazonas and Roraimastates), E Colombia (in the piedmont of the Cordillera Oriental as far N as the Rio Upia drainage in Boyaca Department, including the region of Sierra de la Macarena, E Meta Department, and S to the Coehmani rapids of the Rio Caqueta in the SE of Caqueta Department; it is rare W of the Rio Yari and has been seen on the upper Rio Mesay, opposite the mouth of the Rio Pira-Parana on the right bank of the Rio Apaporis, and the lower right bank of the Apaporis), E Ecuador and NE Peru (restricted to the S of the Rio Napo, extending into N Peru between the rios Putumayo and Amazonas, along the left bank of the Rio Ucayali, and including the basins of the rios Napo, Tigre, Maranén, Pastaza, Pacaya, and Samiria, S as far as the Rio Cushabatay, a tributary of the Rio Ucayali).
Distribution. From the highlands of the Cordillera Oriental in E Ecuador and N Peru, extending E, S of rios Napo and Amazonas, to ¢.70° W, 5° S to the Rio Jurud in W Brazil, and S, W of the Rio Ucayali, to the Rio Pachitea in EC Peru. in Atelidae
Distribution. From the highlands of the Cordillera Oriental in E Ecuador and N Peru, extending E, S of rios Napo and Amazonas, to ¢.70° W, 5° S to the Rio Jurud in W Brazil, and S, W of the Rio Ucayali, to the Rio Pachitea in EC Peru.
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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.