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.
10,950
datasets available to search
ShareScore release 0.9.0
Dataset results
10,950 results for “hosting”
FIG. 4. — Rhinoxenus euryxenus n in Neotropical Monogenoidea. 47. Phylogeny and coevolution of species of Rhinoxenus (Platyhelminthes, Monogenoidea, Dactylogyridae) and their Characiformes hosts (Teleostei, Ostariophysi) with description of four new species
FIG. 4. — Rhinoxenus euryxenus n. sp.; A, holotype (ventral); B, vagina; C, male copulatory organ (MCO); D, hook from pairs 1, 3-7; E, hook from pair 2; F, ventral bar; G, ventral anchor; H, dorsal anchor. Scale bars: A, 100 μm; B-E, 10 μm; F-H, 50 μm.
FIG. 2. — Rhinoxenus anaclaudiae n in Neotropical Monogenoidea. 47. Phylogeny and coevolution of species of Rhinoxenus (Platyhelminthes, Monogenoidea, Dactylogyridae) and their Characiformes hosts (Teleostei, Ostariophysi) with description of four new species
FIG. 2. — Rhinoxenus anaclaudiae n. sp.; A, holotype (ventral); B, male copulatory organ (MCO); C, hook from pair 2; D, hook from pairs 1, 3-7; E, vagina; F, ventral bar; G, dorsal anchor; H, ventral anchor. Scale bars: A, 100 μm; B-E, 10 μm; F-H, 30 μm.
FIG. 7 in Neotropical Monogenoidea. 47. Phylogeny and coevolution of species of Rhinoxenus (Platyhelminthes, Monogenoidea, Dactylogyridae) and their Characiformes hosts (Teleostei, Ostariophysi) with description of four new species
FIG. 7. — Cladogram of hosts groups of Rhinoxenus species constructed from parasitological data and using Characiformes taxa analyzed in the present work. Dashed lines postulate dispersion. Each host group is labeled with its taxonomic epithet followed by the Rhinoxenus species parasitizing its members.
Figure 3 in Development, reproduction and life table parameters of Tetranychus turkestani (Acari: Tetranychidae) on three different host plants
Figure 3 Age-stage-specific life expectancy (exj) of Tetranychus turkestani on: a. cowpea, b. white bean, c. red bean.
Figure 2 in Development, reproduction and life table parameters of Tetranychus turkestani (Acari: Tetranychidae) on three different host plants
Figure 2 Age-specific survival rate (lx), fecundity (mx) and maternity l (x mx) of Tetranychus turkestani on: a. cowpea, b. white bean, c. red bean.
Figure 1 in Development, reproduction and life table parameters of Tetranychus turkestani (Acari: Tetranychidae) on three different host plants
Figure 1 Age-stage-specific survival rate (Sxj) of Tetranychus turkestani on: a. cowpea, b. white bean, c. red bean.
Figure 4 in Development, reproduction and life table parameters of Tetranychus turkestani (Acari: Tetranychidae) on three different host plants
Figure 4 Age-stage-specific life expectancy (vxj) of Tetranychus turkestani on: a. cowpea, b. white bean, c. red bean.
Figure 6 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 6. Secondary structure models of the highly variable proximal part of helix 43 (S6, Fig. 1) in Zygaeninae. All structures are based on thermodynamic folding by minimizing the free energy and have been calculated considering the entire nucleotide sequence of helix 43. The change in the Gibb's free energy (dG) refers to the S6 structure only. Applied ambiguity code: G/A = R, C/U = Y.
Figure 3 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 3. Consensus structure and base pair probability matrix of helix E23-5 (S3, Fig. 1) in Lepidoptera. Nucleotides in circles indicate consistent and/or compensatory substitutions. The size of squares in the grid is proportional to the probability of a base pairing. Note that the species Z. centaureae, Z. laeta and Z. huguenini have been omitted from this analysis because of their deviating secondary structure (compare with Fig. 4).
Figure 2 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 2. Distribution of pairwise tree edit distances between highly variable SSU rRNA secondary structure areas (S1–S6, Fig. 1) of Zygaenoidea excluding taxa of the subgenus Mesembrynus (top) and of Zygaena species belonging to the subgenus Mesembrynus only (bottom). The extreme values in the Zygaenoidea tree edit distance distribution on the right all involve Z. excelsa, a species showing a highly derived secondary structure in the area S6 (compare with Fig. 6).
Figure 1 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 1. Secondary structure model of the SSU (18S) rRNA gene sequence of Zygaena (Mesembrynus) sarpedon lusitanica Reiss, 1936 (Lepidoptera: Zygaenidae; accession no. AJ830858) and structure variation in the helices E10-1 and E23-12 among species of the subfamily Zygaeninae. Nucleotides in the model are continuously numbered beginning at the 5′-end of the molecule; tick marks identify every tenth base. Light shading indicate helices numbered according to Wuyts et al. (2002). S1–S6 (dark shades) denote areas with variable secondary structure in the subfamily Zygaeninae. Roman numerals specify the domains I, II, III and IV. The following ambiguity code has been applied: A/C = M, C/U = Y, G/A = R.
Figure 7 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 7. Neighbour-joining tree based on structural differences in the variable areas S1–S6 (compare with Fig. 1) of the small-subunit (18S) rRNA in taxa of the genus Zygaena. The topology is rooted with Reissita simonyi and Epizygaenella caschmirensis as outgroup. Taxa of the subgenus Mesembrynus are indicated by shading. Numbers in parentheses specify the number of species in a particular group.
Figure 5 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 5. Consensus structure and base pair probability matrix of the proximal part of helix 43 (S6, Fig. 1) in Lepidoptera. Nucleotides in circles indicate consistent and/or compensatory substitutions. The size of squares in the grid is proportional to the probability of a base pairing. Note that the unpaired nucleotides C and G in the helix will most likely bind in individual structures having this specific nucleotide combination, but non-Watson–Crick pairings are too frequent in the alignment for assuming a generally nucleotide interaction at this position in the consensus structure.
Fig. 3 in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil
Fig. 3. Correlation between the standard length of Pygocentrus nattereri and the number of branchiurans (intensity of infestation) in lakes and an oxbow lake at the rio Araguaia, State of Goiás, Amazon basin. (rs= 0.2397, p= 0.0001).
Fig. 2. The circle outlines a in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil
Fig. 2. The circle outlines a tumor (a) observed on Pygocentrus nattereri, possibly caused by the action of the isopod Braga patagonica (b).
Fig. 1 in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil
Fig. 1. Relative frequencies (%) of attachment sites of branchiurans on Pygocentrus nattereri (Serrasalminae) in the Amazon basin.
Figure 1 in Phylogeny-based species delimitations and the evolution of host associations in symbiotic zoanthids (Anthozoa, Zoanthidea) of the wider Caribbean region
Figure 1. Phylogeny of Caribbean symbiotic zoanthids based on the internal transcribed spacer (ITS) region of the rRNA nuclear gene. Support values are 100 pseudoreplicate maximum likelihood (ML) bootstrap values followed by three million iteration Bayesian posterior probabilities. The clades of symbiotic species are colour coded according to their host associations. The information presented in parentheses after the specimens collected for this study includes: the colour of the zoanthid, presence of Symbiodinium, host taxa, and individual identifier (which includes the collection location).
Figures 83–87 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 83–87. (83) P. greenwoodi head; (84) P. greenwoodi mandibles; (85) P. xanthocephalus sp. nov. head. Scale bar = 100 Mm; (86) P. greenwoodi clypeus; (87) P. xanthocephalus sp. nov. clypeus. Scale bar = 50 Mm.
Figure 94 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figure 94. Comparison of head shape between P. athysanus sp. nov. (Fig. 60) and P. proximus Wiebes (Fig. 62).
Figures 63–70 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 63–70. Antennae (females). (63) P. astrabocheilus sp. nov.; (64) P. proximus; (65) P. imperialis; (66) P. macrocainus sp. nov.; (67) P. greenwoodi; (68) P. cuneatus; (69) P. xanthocephalus sp. nov.; (70) P. athysanus sp. nov.
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.