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Fig. 7. T. thermophila cells immunostained with the antiserum against component B in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 7. T. thermophila cells immunostained with the antiserum against component B of epiplasm. DF – staining around the deep fibers. Other explanations as in Fig. 1. Bar: 10 µm.
Fig. 2 in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 2. Localization of nuclei in control and roscovitine treated T. tetrmophila. The cells were immunostained with the anti-centrin 20H5 antibody and stained with DAPI. A and B – control cells in the VI stage of morphogenesis, and early cytokinesis, respectively; C and D – roscovitine treated cells (4 h) in the VI stage of morphogenesis and in cytokinesis respectively. Arrows – micronuclei (in the C micronucleus in opisthe is out of focus). Bar: 10 µm.
Fig. 4. Postdivider cells after 5.5 h in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 4. Postdivider cells after 5.5 h of roscovitine treatment. Cells were immunostained with anti-centrin 20H5 antibody. A and A' – ventral and dorsal views of the same proter cell with remnants of the OA2; B–C opisthe cells, B – opisthe with ARF on dorsal side, C – opisthe with remnants of oral structures; D and D' – ventral and dorsal views of the same cell; E and E' – ventral and dorsal views of the same opisthe during pinching off the OA. Other explanations as in Fig. 1. Bar: 10 µm for A–E'.
Fig. 5 in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 5. Mean cell sizes, positions of OA1, OA2 and fission zone in control and in roscovitine treated cells. Upper panel: early and late control dividers, lower panel: early dividers after 3.5 h roscovitine treatment, late dividers after 3.5 and 5.5 h roscovitine treatment. The shape of cells is represented by elipses. Solid horizontal lines – cells "equator", dotted horizontal lines – positions of the fission furrow. All sizes and distances were drawn to the same scale. Bar: 10 µm. The measurements represent means of at least 10 specimens for each cell sample.
Fig. 6 in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 6. Correlation of length of proters and shift of the fission zone in relation to OA2 induced by roscovitine in late dividers. The shift of the fission zone was measured as a difference between length of the proters and distance from cell apex to the anterior end of the OA2 (ordinate). Each point in this diagram represent individual cell. Open symbols – untreated cells, close symbols – cells treated with roscovitine for 3.5 and 5.5 h (pooled).
Fig. 10 in Effects of Roscovitine on Schedule of Divisional Morphogenesis, Basal Bodies Proliferation and Cell Divisions in Tetrahymena thermophila
Fig. 10. Western blot of T. thermophila fractions with monoclonal antibody anti-cdc14A. H – homogenate, S – supernatant, C – cortical fraction (pellet).
Figure 3 in Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond
Figure 3. Correlation between amount of precipitation and breeding success at Bager Pond, 2008–2011. Data points are Early and Late groups in 4 years.
Figure 9 in Effects of salinity tolerances on survival and life history of 2 cladocerans
Figure 9. Body morphology parameters curves of S. mucronata for the various salt concentrations (±standard error) due to time (with 95% confidence interval).
Figure 8 in Effects of salinity tolerances on survival and life history of 2 cladocerans
Figure 8. Growth rate of S. vetulus under different salt concentrations (with regression equations) in 8-day experiments (with 95% confidence interval).
Figure 7 in Effects of salinity tolerances on survival and life history of 2 cladocerans
Figure 7. Growth rate of S. mucronata under different salt concentrations (with regression equations) in 8-day experiments (with 95% confidence interval).
Figure 4 in Effects of salinity tolerances on survival and life history of 2 cladocerans
Figure 4. Total progeny of S. vetulus under different salt concentrations (with regression equations) in 8-day experiments (with 95% confidence interval).
Figure 2 in Effects of salinity tolerances on survival and life history of 2 cladocerans
Figure 2. Survivorship curves of S. vetulus under different salt concentrations (with regression equations) in 8-day experiments (n = 6; ±standard error; P <0.05).
Figure 3 in Effect of land cover on biodiversity and composition of a soil macrofauna community in a reclaimed coastal area at Yancheng, China
Figure 3. The dendrogram of cluster analysis on soil macrofauna from different habitats with Bray–Curtis similarity by paired groups method (A: Uncultivated land; B: Bulrush land; C: Wheat farm; D: Poplar forest; E: Metasequoia forest).
Figure 2 in Effect of land cover on biodiversity and composition of a soil macrofauna community in a reclaimed coastal area at Yancheng, China
Figure 2. One-way ANOVA on taxonomic richness and abundance, Margalef 's richness index (R) and Shannon-Weaver diversity index (H') among different habitats (Mean ± SE). The means with different scripts are significantly different by SNK test, α = 0.05.
Figure. Mean pre-adult development time (in days) values for all strains. Vertical bars denote 0.95 confidence intervals. in Effects of artificial migration of susceptible individuals on resistance and fitness of a fenitrothion-resistant strain of Musca domestica (L.) Diptera
Figure. Mean pre-adult development time (in days) values for all strains. Vertical bars denote 0.95 confidence intervals.
Figure 3. The effective population size through recent time for 3 in Comparative analyses of past population dynamics between two subterranean zokor species and the response to climate changes
Figure 3. The effective population size through recent time for 3 clades of Gansu zokor (Eospalax cansus).
Figure 1 in Capturing Males of Pestiferous Fruit Flies (Diptera: Tephritidae): Is the Combination of Triple-Lure Wafers and Insecticidal Strips as Effective as Standard Treatments?
Figure 1. Captures of Ceratitis capitata, Bactrocera dorsalis, and Bactrocera cucurbitae males in Jackson traps baited with standard lures or triple-lure wafers over a 12-week interval in October-December, 2013, in a coffee field near Haleiwa, Oahu. Symbols represent mean values of 15 traps; error bars represent 1 SE.
Fig. 1 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 1. Distributions of breeding and wintering populations of S. m. borealis, S. m. dresseri, and S. m. sedentaria in North America and Greenland. Populations of S. m. borealis are wintering in two areas in the pictured region; one in Southwest Greenland and one in East Canada (Newfoundland and Labrador). Individuals wintering in Southwest Greenland migrate to breed in West Greenland or Arctic Canada, whereas individuals wintering in East Canada have breeding areas in Arctic Canada (illustrated by the different direction of the red diagonal lines). For S. m. dresseri the breeding and wintering ranges overlap in one area that covers Newfoundland and Labrador as well as the northeastern part of the US, as shown by the grey horizontal lines. The subspecies S. m. sedentaria has its year-round residence in the Hudson Bay area as shown by the blue vertical lines. Dark stars mark the sampling locations of eiders in this study, whereas the white star marks the sampling location of eiders by Tourangeau et al. (2018). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 3. Prevalences of the cestodes Lateriporus sp. (A) and Microsomacanthus spp. (B), and the acanthocephalan Profilicollis sp. (C) in common eiders. Abbreviations: bor, CD = S. m. borealis, Cape Dorset; bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; sed, BI = S. m. sedentaria [data published in Tourangeau et al. (2018)]. n-m = non-migratory, po-m = post-migratory, prm = pre-migratory. Letters describe significant differences between groups: if two groups share a letter, there is no significant difference in their prevalences.
Fig. 2 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 2. Examples of gastrointestinal parasites retrieved from common eiders in this study. (A) The trematode Notocotylus sp., (B) the cestode Lateriporus sp., (C) the acanthocephalan, Profilicollis sp. (D) microphallid trematodes, and (E) Microsomacanthus spp. cestodes.
ScienceDex guides
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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.