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 5 in Addressing biases in replacement series: the importance of reference density selection for interpretation of competition outcomes
Figure 5. Relative biomass of Setorio foberi:maize replacement series from experiment 1 (left) and experiment 2 (right) with densities based in inflection point (A and B), maximum biomass (C and D), and equal N uptake (E and F). Black circles represent maize relative biomass, white circles represent S. foberi relative biomass, and gray diamonds represent relative yield total biomass (RYT). Dotted line represents a relative biomass of 1 for all the proportions. The points and error bars represent data means and standard errors.
FIGURE 3 in Histology of spinosaurid dinosaur teeth from the Albian-Cenomanian of Morocco: Implications for tooth replacement and ecology
FIGURE 3. (A-E) Teeth SNSB-BSPG 2008 XXXVII 1a–5a in mesial (left) and lingual (right) view. All scale bars equal 1 cm.
Figure 4 in Replacement level of rubber seed cake for soybean meal on the growth of Japanese quail
Figure 4. Survivability (%) of the growing quail under different dietary treatments (D , D , D , D and D = Treatments, see Table 1).
Figure 6 in Replacement level of rubber seed cake for soybean meal on the growth of Japanese quail
Figure 6. Regression for the equation of, y = a + bx; where, y= feed intake, x= the inclusion rate of RS in the diet in place of soybean meal, and b= regression co-efficient and a= intercept. D0= Diet containing 20% soybean meal and 4% soybean oil (control diet), D1= Diet, where 12.5% of soybean meal and 25% of soybean oil has been replaced by RS; D2 = Diet, where 25% of soybean meal and 50% of soybean oil has been replaced by RS; D3 = Diet, where 37.5% of soybean meal and 75% of soybean oil has been replaced by RS; D4 = Diet, where 50% of soybean meal and 100% of soybean oil has been replaced by RS.
Figures 1–2 in Neospastis camellia S. Wang, nom. nov. (Lepidoptera: Xyloryctidae), a replacement name of N. simaona in China
Figures 1–2. Adults of Neospastis camellia S. Wang, nom. nov. 1. Paratype, male (a. Head in lateral view; b. Head in front view). 2. Paratype, female (a. Head in lateral view; b. Head in front view). Scale bars: 1–2 = 2.0 mm; a–b = 0.2 mm.
Figures 5–13 in Neospastis camellia S. Wang, nom. nov. (Lepidoptera: Xyloryctidae), a replacement name of N. simaona in China
Figures 5–13. Immature stages of Neospastis camellia S. Wang, nom. nov. 5. Eggs. 6–8. Larvae. 6. 1st instar larva. 7. 2th instar larva. 8. 4th instar larva. 9. 6th instar larva. 10. Pupae. 11–13. Feeding behavior.
Figures 3–4 in Neospastis camellia S. Wang, nom. nov. (Lepidoptera: Xyloryctidae), a replacement name of N. simaona in China
Figures 3–4. Genitalia of Neospastis camellia S. Wang, nom. nov. 3. Male genitalia, paratype, slide No. TZL19804♂ (a. Paratype, enlarged lateral lobes of juxta, slide No. TZL20454). 4. Female genitalia, paratype, slide No. TZL19805♀ (a. Enlarged signum). Scale bars: 3–4 = 0.5 mm; a = 0.2 mm.
Disk replacement log file examples from a very large RAID disk system for predictive maintenance analysis
<p>README.txt</p> <p>Maintenance example belonging to: </p> <p> The MANTIS Book: Cyber Physical System Based Proactive Collaborative Maintenance<br> Chapter 9, The Future of Maintenance (2019).<br> Lambert Schomaker, Michele Albano, Erkki Jantunen, Luis Lino Ferreira<br> River Publishers (DK)<br> ISBN: 9788793609853, e-ISBN: 9788793609846, https://doi.org/10.13052/rp-9788793609846</p> <p>The figure .pdf did not make it into the book. Here are the raw data, processed <br> logs and .gnu script to produce it.</p> <p>Data: event logs on disk failure in two racks of a huge RAID disk system (2009-2016).</p> <p>disks1.raw<br> disks2.raw</p> <p>Event logs to RC-filtered time series:<br> RC-filt-disks-log.c <br> do-RC-filter-to-make-spikes-more-visible (bash script)<br> --><br> disks1.log<br> disks2.log</p> <p>Constant (horizontal line) indicating the level where users experienced system-down time<br> Disrupted-operations-threshold</p> <p>disk-replacement-log.gnu<br> disk-replacement-log.pdf<br> </p>
Reconstruction of the skeletons of Struthiomimus altus (left) and Ornitholestes hermanni (right). Struthiomimus 1/10, Ornitholestes 1/6 natural size, The Ornitholestes restoration replaces the original restoration by Osborn in 1903 which is very faulty. The Struthiomimus, Amer. Mus. 5339, mount has the distal end of the tail restored from Amer. Mus. 5355; dotted vertebra from Amer. Mus. 5262, In both restorations the pollex is too closely appressed to the other digits, see Fig. 3. in Skeletal Adaptations of Ornitholestes, Struthiomimus, Tyrannosaurus
Reconstruction of the skeletons of Struthiomimus altus (left) and Ornitholestes hermanni (right). Struthiomimus 1/10, Ornitholestes 1/6 natural size, The Ornitholestes restoration replaces the original restoration by Osborn in 1903 which is very faulty. The Struthiomimus, Amer. Mus. 5339, mount has the distal end of the tail restored from Amer. Mus. 5355; dotted vertebra from Amer. Mus. 5262, In both restorations the pollex is too closely appressed to the other digits, see Fig. 3.
Figure 1 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?
Figure 1. Map of collecting localities of mud-dauber wasps' nest aggregations in Seychelles (2016): (1) Anse Marie- Louise, Mahé; (2) Anse Possession, Praslin; and (3) Anse La Passe, Silhouette.
Figure 5 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?
Figure 5. Nest of the mud dauber wasp Sceliphron fuscum (Sphecidae) used by Megachile (Callomegachile) disjuncta (Megachilidae). (A) Nest. The red arrows show cells with black, wax-like substance around entrances used by M. (C.) disjuncta females for nesting. Scale bar = 10 mm. (B-D) Leaf rolls of M. (C.) disjuncta extracted from mud cells of S. fuscum. Scale bar = 5 mm. (Photos: Yulia S. Kolosova).
Figure 4 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?
Figure 4. Native and introduced hymenopteran species (successors and a kleptoparasite) associated with nests of the mud dauber wasp Sceliphron fuscum (Sphecidae) in Seychelles (2016). (A, B) Female of Megachile (Callomegachile) disjuncta (Megachilidae). (C, D) Male of M. disjuncta. (E, F) Chrysis lincea (Chrysididae). (G, H) Chalybion madecassum (Sphecidae). (I, J) Rhynchium brunneum (Vespidae). Scale bar = 5 mm. (Photos: Elizaveta A. Spitsyna).
Fig. 1 in Epidemiology of a major honey bee pathogen, deformed wing virus: potential worldwide replacement of genotype A by genotype B
Fig. 1. Relative proportion of DWV genotype A and B reads in publicly available NCBI transcriptome datasets of honey bees, V. destructor mites and bumble bees.
Fig. 2 in Epidemiology of a major honey bee pathogen, deformed wing virus: potential worldwide replacement of genotype A by genotype B
Fig. 2. First published records of DWV genotype B in Varroa destructor (closed box) or in Apis mellifera (red boxes: pre-2010; open boxes: 2010 onwards) from a country or geographic region; citations are in Table 3. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Epidemiology of a major honey bee pathogen, deformed wing virus: potential worldwide replacement of genotype A by genotype B
Fig. 4. Temporal change in the proportion of DWV-A to DWV-B across our own datasets (a) (prevalence in Fig. 3); in published datasets (b) (UK data in Kevill et al. (2021); continental USA data in Ryabov et al. (2017); and Hawaii data in Grindrod et al. (2021)); and (c) in NCBI NGS honey bee datasets of Fig. 1 presented by geographic origin.
Fig. 3 in Epidemiology of a major honey bee pathogen, deformed wing virus: potential worldwide replacement of genotype A by genotype B
Fig. 3. Temporal change in the prevalence of DWV-A and DWV-B in honey bees in three original datasets separated by 5–6 years from the same sampling localities in the UK (individual honey bees collected at flowers), Germany (pooled honey bees from collapsing colonies) and Italy (NGS reads from pooled or individual honey bees); Germany 2019 samples were summed 2019–2020; Italy 2011 samples were summed 2009–2013 and Italy 2019 samples were summed 2018–2020.
Fig. 8 in Phosphate replicated and replaced microstructure of molluscan shells from the earliest Cambrian of China
Fig. 8. Ilsanella? rozanovi Wang,1994. Specimen NIGP Mo 131358 from sample yd96924−8,upper phosphatic bed of the Zhongyicun Member,Baizai of Xundian in the eastern Yunnan,Meishucunian. A. Lateral view. B. Apical view. C. Enlargement of place shown by arrow in B,note cross section of prism replicated by internal mould. D. Enlargement of place shown by arrow in C.
Fig. 6 in Phosphate replicated and replaced microstructure of molluscan shells from the earliest Cambrian of China
Fig. 6. Archaeospira ornata Yu,1979. A. Specimen NIGP Mo 131370 from sample yd96923−10,upper part of the Dahai Member,Dahai of Huize in the eastern Yunnan,Meishucunian. Apical view (A 1); lamello−fibrillae at the apex (A2). B. Specimen NIGP Mo131370A from sample yd9649−2,upper phosphatic bed of the Zhongyicun Member,Yulu of Huize in the eastern Yunnan,Meishucunian. Lamello−fibrillae of the shell wall. C. Specimen NIGP Mo 131365 from yd96923−10, upper part of the Dahai Member, Dahai of Huize in the eastern Yunnan, Meishucunian (note fibrous structure).
Fig. 5 in Phosphate replicated and replaced microstructure of molluscan shells from the earliest Cambrian of China
Fig. 5. Latouchella cf. korobkovi Vostokova,1962. Specimen NIGP Mo 131371 from yd96924−8A upper part of the Dahai Member,Dahai of Huize in the eastern Yunnan, Meishucunian. A. Lateral view. B, C. Enlargement of place shown by arrow in B, note lamello−fibrillar structure.
Fig. 3 in Phosphate replicated and replaced microstructure of molluscan shells from the earliest Cambrian of China
Fig. 3. Watsonella yunnanensis (He and Yang,1982). Specimen NIGP Mo 131363 from sample yy9649−1,upper phosphatic bed of the Zhongyicun Member, Yulu of Huize in the eastern Yunnan, Meishucunian. A. Lateral view. B, C. Lamello−fibrillar structure. D. Enlargement of C.
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.