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.
403
datasets available to search
ShareScore release 0.9.0
Dataset results
403 results for “captivity”
Fig. 9 in Captive individuals of endangered Philippine raptors maintain native feather mites (Acariformes: Pterolichoidea) species
Fig. 9. Pseudogabucinia nisaeti sp. n. details. A – opisthosoma of male, ventral view, B–D – genu, tibia and tarsus I–III of male, respectively, dorsal view, E – tibia and tarsus IV of male, F, G – tibia and tarsus III and IV of female, respectively, G – tibia and tarsus IV of female, H – spermatheca and spermaducts.
Fig. 10 in Captive individuals of endangered Philippine raptors maintain native feather mites (Acariformes: Pterolichoidea) species
Fig. 10. Phylogenetic tree of EF1 sequences from pterolichoid feather mites available in GenBank (black) with feather mites from Philippine raptors studied (red); tree topology was reconstructed in the RaxML program. Values of the statistical support (are given above the branches if they exceed 65%) were computed by following methods: Mr. Bayes/ML (by RaxML) and NJ (by Mega6). ABGD and GMYC marks represent significant nodes (p <0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Molecular characterization of Blastocystis sp. in captive wildlife in Bangladesh National Zoo: Non-human primates with high prevalence and zoonotic significance
Fig. 1. Phylogenetic tree of the Blastocystis sp. isolates and reference SSU rRNA gene sequences from GenBank based on maximum likelihood analysis. The tree was rooted on Karotomorpha sp. and Protoopalina intestinalis. Bootstrap values> 50% from 1,000 replicates are shown on the nodes. Reference sequences from GenBank have accession number and host designation. The isolates of seven subtypes, with their host designations, are indicated by triangle shape.
Fig. 1. Phylogenetic relationship among the Enterocytozoon bieneusi groups. The relationship between the E in New genotypes and molecular characterization of Enterocytozoon bieneusi in captive black bears in China
Fig. 1. Phylogenetic relationship among the Enterocytozoon bieneusi groups. The relationship between the E. bieneusi genotypes identified in this study and other known genotypes deposited in GenBank was inferred by neighbor-joining analysis of ITS sequences based on genetic distance using the Kimura-2-parameter model. The numbers on the branches represent percent bootstrapping values from 1000 replicates, with more than 50% shown in the tree. Each sequence is identified by its accession number, genotype designation, and host origin. Genotypes marked with black rhombuses and black triangles are novel and known genotypes identified in this study, respectively.
Figures 13-14 in Predation strategies of Harpactor angulosus (Lepeletier & Serville, 1825) (Hemiptera: Reduviidae) on Cladomorphus phyllinus Gray, 1835 (Phasmatodea: Phasmatidae) in captivity
Figures 13-14. Fifth instar nymph of Harpactor angulosus feeding on the membranous neck of a Cladomorphus phyllinus female. / Ninfa de quinto estadio de Harpactor angulosus alimentándose del
Figures 10-12 in Predation strategies of Harpactor angulosus (Lepeletier & Serville, 1825) (Hemiptera: Reduviidae) on Cladomorphus phyllinus Gray, 1835 (Phasmatodea: Phasmatidae) in captivity
Figures 10-12. Nymphs of Harpactor angulosus feeding on Cladomorphus phyllinus. 10-11. Fourth instar nymph on a male of C. phyllinus. 12. Third instar nymph feeding on the lateral abdominal suture of a C. phyllinus male. / Ninfas de Harpactor angulosus alimentándose de Cladomorphus phyllinus. 10-11. Ninfa de cuarto estadio en un macho de C. phyllinus. 12. Ninfa del tercer estadio alimentándose de la sutura abdominal lateral de un macho de C. phyllinus.
Figures 5-8. Harpactor angulosus. 5-6 in Predation strategies of Harpactor angulosus (Lepeletier & Serville, 1825) (Hemiptera: Reduviidae) on Cladomorphus phyllinus Gray, 1835 (Phasmatodea: Phasmatidae) in captivity
Figures 5-8. Harpactor angulosus. 5-6. Fourth and fifth instar nymphs feeding in a leaf and in a branch of guava, respectively. 7. Aspect of the leaf after having been pierced by H. angulosus showing the yellow spots and the brown excrement drop.8. Male in a powder-puff branch. / 5-6. Ninfas de cuarto y quinto estadio alimentándose en una hoja y en una rama de guayaba, respectivamente. 7. Aspecto de la hoja después de haber sido perforada por H. angulosus mostrando las manchas amarillas y la gota de excremento marrón. 8. Macho en una rama de borlas.
Figure 4 in Predation strategies of Harpactor angulosus (Lepeletier & Serville, 1825) (Hemiptera: Reduviidae) on Cladomorphus phyllinus Gray, 1835 (Phasmatodea: Phasmatidae) in captivity
Figure 4. Female of Cladomorphus phyllinus being preyed by a fifth instar nymph of Harpactor angulosus. / Hembra adulta de Cladomorphus phyllinus presa de una ninfa de quinto estadio de Harpactor angulosus.
Figure 1 in Reproduction, postnatal development, and social behavior of Ellobius lutescens Thomas 1897 (Mammalia: Rodentia) in captivity
Figure 1. Development of E. lutescens pups (A- newly born, B- 7 days, C- 14 days, D- 21 days, E- 28 days, F- 42 days, G- 56 days, H- 70 days, I- 84 days).
Figure. Distribution of body mass of 22 edible dormouse juveniles at the last weighing before hibernation. in Changes in body mass of postweaning juveniles of the edible dormouse, Glis glis (L.), in captivity
Figure. Distribution of body mass of 22 edible dormouse juveniles at the last weighing before hibernation.
Figure 3 in Tolerance limit of physicochemical water parameters in giant freshwater prawn (Macrobrachium rosenbergii) in a captive condition
Figure 3. Six replicates of the mean of cold temperature critical limit (maximum and minimum) subject to M. rosenbergii.
Figure 6 in Tolerance limit of physicochemical water parameters in giant freshwater prawn (Macrobrachium rosenbergii) in a captive condition
Figure 6. Variation of different temperatures (29.8 °C, 20.9 °C, 16.9 °C, and 13.9 °C) in the experimental tank.
Fig. 2 in Toxoplasma gondii infection in European mouflons (Ovis musimon) and captive wild felines from Puebla, M�exico
Fig. 2. Representative PCR-RFLP pattern of T. gondii for SAG3 gene. Single and mixed infections in lions and mouflons tissues were observed. A. PCR for the SAG3 locus of lion 1 (L1, spleen), mouflon 1 (M1, brain) and mouflon 2 (M2, liver) samples. B. A triple infection is highlighted (yellow box). Resulting genotypes are specified at the bottom. In silico digestion was done by www.benchling.com. Reference strains sequences GT1, TGGT1_308020; Me49, TGME49_308020; VEG, TGVEG_308020 are available at www.toxodb.org. MW: molecular weight marker; RH and ME49 are reference strains, type I and II, respectively; M: mouflon, L: lion. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Toxoplasma gondii infection in European mouflons (Ovis musimon) and captive wild felines from Puebla, M�exico
Fig. 1. Toxoplasma gondii infection in captive mouflons in 2011 and 2012. A. Anti-T. gondii frequency distribution in fifty-five sera of mouflons sampled in 2011; black arrows indicate positive samples as determined by their position to the right of the normally distributed values of the left population. B. One year later, 41/55 original mouflons were captured, bled, and re-tested for antibodies against this parasite. The cut-off point used was 1.0 RI (dotted lines), which separated the negative population (left) from the positive cases. C. Three mouflons remained positive, five became negative, and four seroconverted positive in 2012 (red, green and blue dots, respectively); one mouflon is on the cut-off (orange dot). D. Immunohistochemistry for T. gondii in tissues from in the spleen of mouflon 1, where an immunopositive cumulus of tachyzoites can be seen (blue arrow). The nuclei of resident lymphocytes and dendritic cells were contrasted with Meyer's hematoxylin. Bar: 50 μm. R = Pearson correlation. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Review on parasites of wild and captive giant pandas (Ailuropoda melanoleuca): Diversity, disease and conservation impact
Fig. 1. Distribution of wild giant pandas in six mountain regions (Qinling, Minshan, Qionglai, Liangshan, Daxiangling and Xiaoxiangling) in three Provinces (Gansu, Shaanxi, and Sichuan) of China. Adapted from Wang et al. (2018).
Fig. 3 in Captive breeding program for Scinax alcatraz (Anura: Hylidae): introducing amphibian ex situ conservation in Brazil
Fig. 3. Breeding of Scinax alcatraz at São Paulo Zoo. a) A pair in amplexus. b) Eggs deposited in the water. c) Maintanance of tadpoles in plastic pots with filtered water. d) Post-metamorph individuals (SVL x=12.49 mm). Photos by Cybele Lisboa.
Fig. 6 in Captive breeding program for Scinax alcatraz (Anura: Hylidae): introducing amphibian ex situ conservation in Brazil
Fig. 6. Range of environmental conditions (relative humidity and air temperature) most favorable for reproduction of Scinax alcatraz in captivity.
Fig. 5 in Captive breeding program for Scinax alcatraz (Anura: Hylidae): introducing amphibian ex situ conservation in Brazil
Fig. 5. Correlation between breeding events of Scinax alcatraz and environmental conditions (a) relative humidity and (b) air temperature from August 2013 to December 2017. Pearson product-moment Correlation Coefficient: r = 0.323; p <0.001; N = 732.
Fig. 2 in Captive breeding program for Scinax alcatraz (Anura: Hylidae): introducing amphibian ex situ conservation in Brazil
Fig. 2. Laboratory colony of Scinax alcatraz at Sao Paulo Zoo. a) Aquariums for maintanance of juveniles and adults. b) Plastic cups with filtered water and submerged plants for refuge. Photos by Cybele Lisboa.
Fig. 5 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 5. Micrograph of the brain on infected jaguar. Schizonts inside macrophages contain numerous round to oval 1–2 μm diameter basophilic organisms (merozoites). HE.
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.