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.
6,383
datasets available to search
ShareScore release 0.9.0
Dataset results
6,383 results for “isolates”
Fig. 1 in Isolation of native strains of entomopathogenic fungi from agricultural soils of northeastern Mexico and their virulence on Spodoptera exigua (Lepidoptera: Noctuidae)
Fig. 1. Phylogenetic tree reconstructed from internal transcribed spacer sequences of the isolates compared with referenced internal transcribed spacer sequences deposited in the NCBI GenBank. The phylogram size bar represents a 1% sequence divergence. Labelled branches represent referenced internal transcribed spacer sequences.
Fig. 12 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 12. Threats to the isolated hill forests and Cnemaspis species in study areas in Sri Lanka. (A) Illegal forest clearing, (B) fire- wood collection for tea factory, (C) granite mining activities, (D) agricultural fields in slopy areas, (E) tea plantation and highly crowded anthropogenic habitat, and (F) a landslide in mountain areas. Photos: Suranjan Karunarathna and Madhava Botejue.
Fig. 11 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 11. General habitats of Cnemaspis kawminiae sp. nov. at Mandaramnuwara, Nuwara-Eliya District, Sri Lanka. (A) Complete view of the granite hill at roadside, (B) small granite cave close to the stream, and (C) granite rock wall along the road. Photos: Madhava Botejue.
Fig. 10 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 10. Holotype male of Cnemaspis kawminiae sp. nov. (NMSL 2018.18.01) in life in-situ. (A) Dorsal view of the full body, and (B) dorsolateral view with labial coloration. Photos: Madhava Botejue.
Fig. 8 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 8. General habitat of Cnemaspis dissanayakai sp. nov. at Dimbulagala isolated hill forest, Polonnaruwa District, Sri Lanka. (A) Complete view of the mountain, (B) abandoned ancient cave building in Kosgahaulpatha, and (C) deep and tall granite tunnel. Photos: Madhava Botejue and Ashan Geeganage.
Fig. 5 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 5. General habitat of Cnemaspis kotagamai sp. nov. at Bambaragala isolated forest hill, Ratnapura District, Sri Lanka. (A) Rock outcrop habitat, (B) abandoned cave building, and (C) deep and tall granite tunnel. Photos: Madhava Botejue.
Fig. 7 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 7. Holotype male of Cnemaspis dissanayakai sp. nov. (NMSL 2018.20.01) in life in-situ in Dimbulagala. (A) Dorsal view of the full body, and (B) ventral view with dirty white coloration. Photos: Suranjan Karunarathna.
Fig. 9 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 9. Holotype male of Cnemaspis kawminiae sp. nov. (NMSL 2018.18.01). (A) Dorsal head, (B) lateral head, (C) ventral head, (D) homogeneous dorsal scales, (E) scales on lateral surface of trunk, (F) smooth ventral scales, (G) cloacal characters with precloacal pores and femoral pores, (H) lamellae on manus, (I) lamellae on pes, (J) smooth dorsal scalation of tail, (K) lateral side of tail, and (L) very small subcaudals. Photos: Suranjan Karunarathna.
Fig. 4 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 4. Holotype male of Cnemaspis kotagamai sp. nov. (NMSL 2018.07.01) in life in-situ in Bambaragala. (A) Dorsal view of the full body, and (B) ventral view with scattered yellow coloration. Photos: Suranjan Karunarathna.
Fig. 6 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 6. Holotype male of Cnemaspis dissanayakai sp. nov. (NMSL 2018.20.01). (A) Dorsal head, (B) lateral head, (C) ventral head, (D) homogeneous dorsal scales, (E) scales on lateral surface of trunk, (F) smooth ventral scales, (G) cloacal characters with precloacal pores and femoral pores, (H) lamellae on manus, (I) lamellae on pes, (J) smooth dorsal scalation of tail, (K) lateral side of tail, and (L) very small smooth subcaudals. Photos: Suranjan Karunarathna.
Fig. 2 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 2. (A-F) PCA Ordination plots for multivariate morphometric analyses (all pairwise ordination plots for PC1 through PC4 are shown), (G) Scatter plot of PCA between Cnemaspis kotagamai sp. nov. (filled circles), Cnemaspis ingerorum (triangles), and Cnemaspis kallima (filled diamonds), (H) Scatter plot of PCA between Cnemaspis dissanayakai sp. nov. (circles), Cnemaspis latha (filled squares), and Cnemaspis kumarasinghei (stars), (I) Scatter plot of PCA between Cnemaspis kawminiae sp. nov. (squares), Cnemaspis gotaimbarai (filled triangles), and Cnemaspis kumarasinghei (stars).
Fig. 1 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 1. Currently known distribution of Cnemaspis dissanayakai sp. nov. (square) from Dimbulagala; Cnemaspis kawminiae sp. nov. (circle) from Mandaramnuwara; and Cnemaspis kotagamai sp. nov. (triangle) from Bambaragala, Sri Lanka.
Fig. 3 in Three new species of day geckos (Reptilia: Gekkonidae: Cnemaspis Strauch, 1887) from isolated granite cave habitats in Sri Lanka
Fig. 3. Holotype male of Cnemaspis kotagamai sp. nov. (NMSL 2018.15.01). (A) Dorsal head, (B) lateral head, (C) ventral head, (D) heterogeneous dorsal scales, (E) scales on lateral surface of trunk, (F) smooth ventral scales, (G) cloacal characters with precloacal pores and femoral pores, (H) lamellae on manus, (I) lamellae on pes, (J) keeled dorsal scalation of tail, (K) lateral side of tail, and (L) very small smooth subcaudals. Photos: Suranjan Karunarathna.
Figure 3 in Size estimation of Synbranchus marmoratus and Synbranchus madeirae (Teleostei) based on isolated cranial and post-cranial bones
Figure 3. – Map of north-central Chile showing the oceanic islands and Chañaral Island where Pseudocaranx chilensis was sighted.
Figure 2 in Size estimation of Synbranchus marmoratus and Synbranchus madeirae (Teleostei) based on isolated cranial and post-cranial bones
Figure 2. – Individual Pseudocaranx chilensis swimming over the kelp bed at Chañaral Island (depth ~ 5 m).
Fig. 2. Sarcocyst and bradyzoite morphology. A. Isolated S in Sarcocystis rileyi (Apicomplexa) in Anas platyrhynchos in Europe with a potential for spread
Fig. 2. Sarcocyst and bradyzoite morphology. A. Isolated S. rileyi sarcocysts (mean length 5.25 mm) mounted in Aquatex, B. Wet smear of liberated bradyzoites (mean length 13.48 μm) from a sarcocyst of S. rileyi, C. Histological section of a sarcocyst in the musculature of the mallard (scale bar 100 μm), D. Histological section of a S. rileyi sarcocyst in pectoral musculature of male mallard showing densely packed bradyzoites with strongly stained nuclei. Haematoxylin staining. DePeX mounting, (scale bar 100 μm).
Fig. 2 in Workflow of Lotmaria passim isolation: Experimental infection with a low-passage strain causes higher honeybee mortality rates than the PRA-403 reference strain
Fig. 2. Kaplan-Meier survival curves for the experimental groups (C1, control and PRA-403), showing the cumulative mortality over time. Vertical ticks indicate censored observations.
Fig. 1 in Workflow of Lotmaria passim isolation: Experimental infection with a low-passage strain causes higher honeybee mortality rates than the PRA-403 reference strain
Fig. 1. Workflow for the isolation of bee-infecting trypanosomatid parasites from honeybee guts. A. Dissection and tissue processing (steps 1–4), and trypanosomatid culture and expansion (step 5) in liquid or Solid Cultures. B. Growth curve of L. passim PRA-403 strain in decreasing concentrations of 5-Fluorocytosine (1 × 106 μg/ mL-100 μg/mL) to determine the maximum dose for parasite survival. C. Giemsa staining of L. passim C1 (CCP 1). D. Hoescht DNA staining of live L. passim C1 (CCP 1): N, Nucleus; K, Kinetoplast; E, Scanning Electron Microscopy of L. passim C1 (CCP 1) grown in Agar Solid cultures 20 days post-inoculation.
Fig. 5 in Isolated theropod teeth from the Middle Jurassic of Niger and the early dental evolution of Spinosauridae
Fig. 5. Time-calibrated phylogeny of spinosaurids and related theropods. Time-calibrated cladogram elaborated after Carrano et al. (2012) and Allain (2014). The asterisks mark the place of the three basal spinosaurid forms represented only by teeth (Buffetaut et al. 2011; this article). The proposed transition from a plesiomorphic theropod tooth (node 1 and earlier) to a highly derived spinosaurid tooth (node 4) would include a transitional state (represented by MUPE HB-87). 1, Averostra; 2, Tetanurae; 3, Megalosauroidea; 4, Spinosauridae.
Fig. 4 in Isolated theropod teeth from the Middle Jurassic of Niger and the early dental evolution of Spinosauridae
Fig. 4. Dendrogram obtained from the cluster analysis of the theropod teeth. A. Database from Hendrickx and Mateus (2014) and the HB site. The characters used were those proposed by Hendrickx and Mateus (2014) for lateral teeth. HB samples are clustered with Afrovenator and Dubreuillosaurus (black dot). B. Database from Hendrickx and Mateus (2014), the specimens from the HB site, and two basal spinosaurid teeth from the Middle Jurassic TP4 site in Niger (Serrano-Martínez et al. 2015). MUPE HB-118, MUPE HB-125, and MUPE HB-142 remain clustered with Afrovenator and Dubreuillosaurus (black dot), but MUPE HB-87, MUPE TP4-2, and MUPE TP4-3 are clustered with the spinosaurids (white dot).
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.