Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
2,914
datasets available to search
ShareScore release 0.9.0
Dataset results
2,914 results for “replacement”
FIGURE 14 in A morphological and molecular study of Psilops, a replacement name for the Brazilian microteiid lizard genus Psilophthalmus Rodrigues 1991 (Squamata, Gymnophthalmidae), with the description of two new species
FIGURE 14. The appendicular skeleton of Psilops paeminosus (MZUSP 79584). Pectoral (A) and pelvic (B) girdles, in ventral view. Carpal region in ventral (C) and dorsal (D) views. Tarsal region in ventral (E) and dorsal (F) views, respectively. Abbreviations: ac, astragalus-calcaneus; acf, anterior coracoid foramen; ce, centrale; cf, coracoid foramen; cl, clavicle; dc, distal carpal; dt, distal tarsal; epc, epicoracoid; fe, femur; fi, fibula; h, humerus; icl, interclavicle; il, ileum; is, isquium; pa, palmar; pb, pubis; pcf, posterior coracoid foramen; psi, pisiform; ra, radiale; s, sternum; sc, scapulocoracoid; se, suprascapula; ti, tibia; ul, ulnare. Scale bars for A and B = 1mm; scale bars for C-F = 0.25mm.
FIGURE 11 in A morphological and molecular study of Psilops, a replacement name for the Brazilian microteiid lizard genus Psilophthalmus Rodrigues 1991 (Squamata, Gymnophthalmidae), with the description of two new species
FIGURE 11. Hemipenes of Psilops paeminosus (MZUSP 106186, from Gameleira do Assuruá, Bahia) (Clade B—type lineage), in its sulcate, lateral and asulcate faces (A), P. mucugensis (MZUSP 106196, from Miguel Calmon, Bahia) (Clade E), in its sulcate and asulcate faces (B) and, P. seductus (MNRJ 19099, from Jaborandi, Bahia) (Clade A) (C). Scale bars = 1 mm.
FIGURE 4 in A morphological and molecular study of Psilops, a replacement name for the Brazilian microteiid lizard genus Psilophthalmus Rodrigues 1991 (Squamata, Gymnophthalmidae), with the description of two new species
FIGURE 4. Dorsal (top), lateral (middle) and ventral (bottom) views of the head of the holotype of Psilops mucugensis (MZUSP 106188), from Mucugê, Bahia. Scale bar = 1 mm.
FIGURE 10 in A morphological and molecular study of Psilops, a replacement name for the Brazilian microteiid lizard genus Psilophthalmus Rodrigues 1991 (Squamata, Gymnophthalmidae), with the description of two new species
FIGURE 10. Habitat occupied by Psilops seductus on campo cerrado (A), and cerrado sensu stricto (B), at Jaborandi, Bahia.
FIGURE 8 in A morphological and molecular study of Psilops, a replacement name for the Brazilian microteiid lizard genus Psilophthalmus Rodrigues 1991 (Squamata, Gymnophthalmidae), with the description of two new species
FIGURE 8. Dorsal (top), lateral (middle) and ventral (bottom) views of the head of the holotype of Psilops seductus (MNRJ 19099), from Jaborandi, Bahia. Scale bar = 1 mm.
Figs. 7–11 in Replacement Name for the Genus Moorea Ahn (Coleoptera: Staphylinidae)
Figs. 7–11. Pseudocotalpa sonorica, third-instar larva. 7) Ventral view abdomen seg. X; 8) metathoracic leg; 9) lateral view abdomen; 10) protarsungulus-tibiotarsus; 11) head, frontal view.
Figs. 1–6. Pseudocotalpa sonorica, third instar larva. 1 in Replacement Name for the Genus Moorea Ahn (Coleoptera: Staphylinidae)
Figs. 1–6. Pseudocotalpa sonorica, third instar larva. 1) Epipharynx; 2) labium; 3) mandibles left, right dorsal view, mandibles ventral view left, right; 4) last antennal segment, dorsalview; 5) maxillary stridulatory area; 6) left maxilla, central view.
FIGURE 1 in Stachys richardiana nom. nov., a replacement name for S. hypoleuca (Lamiaceae)
FIGURE 1. Lectotype of Stachys palaestina L. var. hypoleuca Benth. (G00684519, © Conservatoire & Jardin botaniques de la Ville de Genève).
Silicate refractory brick waste as quartz sand filler replacement in MOC-based composites: Route to environmentally sustainable construction composites
Open the record for dataset details and reuse information.
Supplementary material 4 from: Liao M, Zeng S-J, Zeng L-Y, Yin H-J, Yan M-L, Zhang C-F, Tang G-D (2024) A new species and a replacement name in Cynanchum (Apocynaceae, Asclepiadeae) from China. PhytoKeys 241: 49-63. https://doi.org/10.3897/phytokeys.241.111499
Specimens of Cynanchum hooperianum, C. longhushanense, C. pingtaoi, and C. pulchellum used for the distribution map
Effects of Locally formulated Milk Replacer on Calf Growth Performance; Physiological, Hematological, and Biochemical Parameters
Open the record for dataset details and reuse information.
Data for "Replacing native grazers with livestock influences arthropods to have implications for ecosystem functions and disease"
Open the record for dataset details and reuse information.
Distribution. Widespread in the upper Amazon, extending from NW Brazil (W of rios Negro, upper Uaupés, and Amazonas-Solimoes) into SE Colombia (S of the Rio Tomo in the Orinoco Basin, and perhaps the upper Rio Guyabero), and S into the Ecuadorian Amazon and NE Peru (to the N bank of the rios Maranon and Amazonas, W as far as the Rio Chinchipe); it occurs also S of the Rio Solimoes in a small area on the lower Rio Purus. Ma's Night Monkey (A. nancymaae) replaces it in a small enclave N of the Rio Maranon between the lower rios Tigre and Pastaza. in Aotidae
Distribution. Widespread in the upper Amazon, extending from NW Brazil (W of rios Negro, upper Uaupés, and Amazonas-Solimoes) into SE Colombia (S of the Rio Tomo in the Orinoco Basin, and perhaps the upper Rio Guyabero), and S into the Ecuadorian Amazon and NE Peru (to the N bank of the rios Maranon and Amazonas, W as far as the Rio Chinchipe); it occurs also S of the Rio Solimoes in a small area on the lower Rio Purus. Ma's Night Monkey (A. nancymaae) replaces it in a small enclave N of the Rio Maranon between the lower rios Tigre and Pastaza.
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.
Distribution. NE Peru, between the rios Amazonas and Yavari, to the right bank of the rios Ucayali and Tapiche as far as the Rio Blanco (upstream of the Rio Ucayali along both sides of the river, to the S of the Rio Blanco, it is replaced by S. illigeri), but it appears again on the right bank of the Rio Ucayali at the headwaters of the Rio Tapiche, a left bank tributary of the Rio Blanco, probably extending E as far as the Rio Yavari, on the border with Brazil. in Callitrichiade
Distribution. NE Peru, between the rios Amazonas and Yavari, to the right bank of the rios Ucayali and Tapiche as far as the Rio Blanco (upstream of the Rio Ucayali along both sides of the river, to the S of the Rio Blanco, it is replaced by S. illigeri), but it appears again on the right bank of the Rio Ucayali at the headwaters of the Rio Tapiche, a left bank tributary of the Rio Blanco, probably extending E as far as the Rio Yavari, on the border with Brazil.
Rest-activity daily rhythm and physical activity levels after hip and knee joint replacement: the role of actigraphy in orthopedic clinical practice.
<p>Elective hip and knee joint replacement for osteoarthritis are cost-effective surgical procedures requiring specific rehabilitation programs. Actigraphy is widely used in both research and clinical practice to study activity patterns with great accuracy and validity but it has never been utilized in orthopedic patients. Therefore, the aim of this study was to objectively assess, through actigraphy, physical activity (PA) levels and rest-activity daily rhythm (RAR) in patients undergoing hip or knee joint replacement and hospitalized for ten days after surgery. Twenty subjects (11 males and 9 females; age: 62.68 ± 10.39 years old; BMI: 29.03 ± 3.92 kg/m2) wore the Actiwatch 2 actigraph (Philips Respironics, Portland, OR) to record both PA levels and RAR for 11 consecutive days and data on subjective scores of pain, by a visual analog scale (VAS), and functional and clinical scores were collected. The following time-points were considered for the statistical analysis: pre-surgery (PRE), the first (POST1), the fourth (POST4) and the tenth (POST10) day after surgery. RAR were processed with the population mean cosinor to describe the rhythm's characteristics (acrophase, amplitude and MESOR) while data on actigraphy-based PA, VAS, and functional clinical scores were compared among PRE, POST1, POST4 and POST 10 with the RM-ANOVA or the non-parametric Friedman test. The day after surgery the subjects had a flattened RAR compared to the other conditions: lower values were detected in POST1 compared to both PRE, POST4 and POST10 for MESOR (<em>p</em> < .0001; η2p = .71, large) and amplitude (<em>p</em> < .0001; η2p = .63, large) while RAR's acrophase (<em>p</em> < .0001; η2p = .61, large) was delayed in PRE (16:45) compared to POST1 (12:42), POST4 (14:38), and POST10 (14:38). PA levels were significantly lower at POST 1 (76.7 ± 33.4) compared to PRE (192.3 ± 91.5; <em>p</em> < .0001 and ES: 1.68, large), POST4 (137.9 ± 45.9; <em>p</em> < .0001 and ES: 1.54, large), and POST10 (131.2 ± 54.3; <em>p</em> < .0001 and ES: 1.21, large) whereas VAS and functional clinical values significantly improved at POST10. Hip and knee joint replacement negatively influenced RAR and PA the first day after surgery but a progressive improvement in the circadian pattern of rest-activity cycle, PA levels, VAS and functional ability was recorded from POST4 to POST10. Actigraphy has the ability to collect real-life data without interfering with clinical practice and give clinicians a new measure of performance that is currently not available. This tool could allow to identify patients with disrupted circadian rhythm and reduced PA in the peri-operative period in orthopedic surgery, and timely intervene on these subjects with personalized rehabilitative intervention.</p>
PASS: An ImageNet replacement for self-supervised pretraining without humans
<p>Computer vision has long relied on ImageNet and other large datasets of images sampled from the Internet for pretraining models. However, these datasets have ethical and technical shortcomings, such as containing personal information taken without consent, unclear license usage, biases, and, in some cases, even problematic image content. On the other hand, state-of-the-art pretraining is nowadays obtained with unsupervised methods, meaning that labelled datasets such as ImageNet may not be necessary, or perhaps not even optimal, for model pretraining. We thus propose an unlabelled dataset <strong>PASS</strong>: Pictures without humAns for Self-Supervision. PASS only contains images with CC-BY license and complete attribution metadata, addressing the copyright issue. Most importantly, it contains no images of people at all, and also avoids other types of images that are problematic for data protection or ethics. We show that PASS can be used for pretraining with methods such as MoCo-v2, SwAV and DINO. In the transfer learning setting, it yields similar downstream performances to ImageNet pretraining even on tasks that involve humans, such as human pose estimation. PASS does not make existing datasets obsolete, as for instance it is insufficient for benchmarking. However, it shows that model pretraining is often possible while using safer data, and it also provides the basis for a more robust evaluation of pretraining methods.<br> <br> A simple download script is here: <a href="https://github.com/yukimasano/PASS/blob/main/download.sh">https://github.com/yukimasano/PASS/blob/main/download.sh</a><br> Visit our webpage here: <a href="https://www.robots.ox.ac.uk/~vgg/research/pass/">https://www.robots.ox.ac.uk/~vgg/research/pass/</a></p>
FIGURES 3–4 in Replacement names for Beckius Dechambre, 1992 and Syrictes Prell, 1936, and validation of Neoryctes Arrow, 1908 (Coleoptera: Scarabaeidae: Dynastinae)
FIGURES 3–4. Dorsal view of males. 3, Kirprellius syrichtus (Fabricius, 1775), new combination (image by Johan Pretorius, https://inaturalist.ca/photos/15855083, Creative Commons). 4, Neoryctes williamsi Cook, Howden, & Peck, 1995, paratype (image by Alain Galant).
FIGURES 1–2 in Replacement names for Beckius Dechambre, 1992 and Syrictes Prell, 1936, and validation of Neoryctes Arrow, 1908 (Coleoptera: Scarabaeidae: Dynastinae)
FIGURES 1–2. Male of Debeckius beccarii (Gestro, 1876), new combination. 1, dorsal view (image by JohnSka, https://commons.wikimedia.org/w/index.php?curid=25049952, Creative Commons); 2, parameres (from Endrődi 1976).
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.