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1,140 results for “Colony”
Fachada Colonial
Source: Objaverse 1.0 / Sketchfab
FIGURES 2–7. Bryozoan colony growth forms. 2 in Diversity of marine bryozoans inhabiting demosponges in northeastern Brazil
FIGURES 2–7. Bryozoan colony growth forms. 2, encrusting patches; 3, encrusting spots; 4, erect articulated; 5, erect delicate branching; 6, erect fenestrate; 7, erect stoloniferan. Scale bars: 5 mm.
Impact of colony size on survival and sanitary strategies in fungus-infected ant colonies
<p>Data of the scientifc paper "Impact of colony size on survival and sanitary strategies in fungus-infected ant colonies"</p>
Genomic Resources for Global and Local Ancestry Estimation in a Captive Baboon Colony
<p>VCF files mapped to <em>Panubis1.0</em> with 881 olive (<em>Papio anubis</em>) and yellow (<em>Papio cynocephalus</em>) baboons from the Southwest National Primate Research Center. VCF files were generated in two separate pipelines, first using Beagle 4.1 and Beagle 5.4 and additionally SHAPEIT5/IMPUTE5 to test if a pedigree-aware software reduced the number of evident phase switch errors. VCFs here have been phased and imputed in their respective pipelines, filtered for imputation accuracy with markers with less than 0.7 confidence removed using BCFTools, and then phase switch corrected using Tractor. Genomic resources (AIMs and Fixed markers) are based off of <em>Panubis1.0 </em>coordinates. Local ancestry estimation completed by RFMix and then phase-switch-corrected using Tractor. </p>
Figure 1 in Comparison of proteomic profiles of the phaeophyte Saccharina japonica thalli proximal to and beneath the front of epiphytic hydrozoan colonies against healthy tissue
Figure 1: Saccharina japonica thallus sections defined as thallus tissue proximal to hydrozoan colonies and tissue at the colony front. The proximal tissues were collected from the 1-cm zone outside the boundary of the colony. The colony-front tissues were obtained from the 1-cm zone under the newly formed front of the colony after removing the hydrozoans. Inset photo shows hydrozoans on the brown alga S. japonica.
Figure 4 in Comparison of proteomic profiles of the phaeophyte Saccharina japonica thalli proximal to and beneath the front of epiphytic hydrozoan colonies against healthy tissue
Figure 4: Sections of two-dimensional gels showing the proteins (arrows) that decreased during hydrozoan colonization. The separated proteins were visualized by silver staining. (A) Distal healthy thallus tissue. (B) Thallus tissue proximal to hydrozoan colonies. (C) Thallus tissue at the colony front.
Figure 3 in Comparison of proteomic profiles of the phaeophyte Saccharina japonica thalli proximal to and beneath the front of epiphytic hydrozoan colonies against healthy tissue
Figure 3: Sections of two-dimensional gels showing the proteins (arrows) that increased most in the thallus tissue proximal to hydrozoan colonies or in the thallus at the colony front, but were not detected in the distal healthy thallus tissue. The separated proteins were visualized by silver staining. (A) Distal healthy thallus tissue. (B) Thallus tissue proximal to hydrozoan colonies. (C) Thallus tissue at the colony front.
Figure 2 in Comparison of proteomic profiles of the phaeophyte Saccharina japonica thalli proximal to and beneath the front of epiphytic hydrozoan colonies against healthy tissue
Figure 2: Two-dimensional gel electrophoresis profiles of lateharvested Saccharina japonica. (A) Distal healthy thallus tissue. (B) Thallus tissue proximal to hydrozoan colonies. (C) Thallus tissue at the colony front. The separated proteins were visualized by silver staining. Numbers attached to the arrows refer to the spot numbers listed in Table 1.
Field measurements performed on Staghorn fern colonies (Platycerium bifurcatum)
<p>This study explores the relationship observed between 'guests' – foreign inhabitants of social colonies – and the density and fecundity of eusocial-like staghorn ferns (<em>Platycerium bifurcatum</em>, Polypodiaceae). Our observations suggest that guests in staghorn colonies have a range of commensal and negative relationships, paralleling those seen in eusocial animal species.</p>
Data used in the study "Application of nanopore sequencing for accurate identification of bioaerosol-derived bacterial colonies"
<p>Data used in the study "Application of nanopore sequencing for accurate identification of bioaerosol-derived bacterial colonies." The datasets contain nanopore and Sanger sequencing data (including the electropherograms) as well as EPI2ME and NGSpeciesID analysis.</p>
Fragmentation and aggregation of cyanobacterial colonies under a cone and plate shear
<p>Brief description of experimental setup: <br>Colonies of the cyanobacteria Microcystis in liquid medium BG-11 are place and a cone-and-plate shear at various values of energy dissipation rate and total biovolume fraction. Brightfield microscopy is perfomed simulanoeusly to the shear flow thorugh the transparente lower plate.</p> <p>Files:<br>rawimages.zip: Raw images (.tiff) for the dataset Fragmentation-eps-5.8m2/s3-phi100ppm. Pixel resolution is 1.63 um/px.<br>features.zip : Processed data from raw images for all data sets are present. Title inform initial distribution ("Bre" = large colonies; "Agg" = single cells), nominal shear rate and total biovolume fraction. Csv files contain background image, detected features using a routine in scikit-image scikit-image and initial parameters. Script for analizing data can be found at https://github.com/FluidLab/CyanoB_Agg_Frag.git</p> <p><br>Contact: Yuri Sinzato - y.z.sinzato@uva.nl / Mazi Jalaal - m.jalaal@uva.nl</p>
Ant Positions, Colony Summary Statistics
<p>x, y coordinates of all ants in genotype A (GS2AAutoDataDistManualNest.mat) and B (GS3BAutoDataDistManualNest.mat)<br> Summary statistics for all colonies of both genotypes (ColonySummaryStatistics_Ulrich.xlsx)</p>
FIGURE 37. Genus et species indet. A, D, F, G, colony 1, GLD4–11, Stn 211 in Bryozoa (Cyclostomata and Ctenostomata) from polymetallic nodules in the Russian exploration area, Clarion - Clipperton Fracture Zone, eastern Pacific Ocean-taxon novelty and implications of mining
FIGURE 37. Genus et species indet. A, D, F, G, colony 1, GLD4–11, Stn 211, respectively showing capitulum with gonozooid floor developing across alveoli, and autozooidal peristomes at periphery; B, C, E, H, I, colony 2, GLD4–12, Stn 255, similar views of a colony with two gonozooid floors developing. Scale bars: A, B, 250 µm; C–H, 100 µm; I, 50 µm.
FIGURE 36. Genus et species indet. A, B, colony 1, GLD4–11, Stn 211 in Bryozoa (Cyclostomata and Ctenostomata) from polymetallic nodules in the Russian exploration area, Clarion - Clipperton Fracture Zone, eastern Pacific Ocean-taxon novelty and implications of mining
FIGURE 36. Genus et species indet. A, B, colony 1, GLD4–11, Stn 211, rotational profiles; C, D, colony 2, GLD4–12, Stn 255, rotational profiles. Scale bars: 250 µm.
FIGURE 14. Walkeria prorepens Kubanin, 1992 in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 14. Walkeria prorepens Kubanin, 1992, Seongsan port, Jeju Island (MBRBK1705). A. Serpulid polychaete tube encrusted on inner side by small Walkeria colony. B. Close-up of small part of A, showing cluster of zooids. C. Live colony around in hole in substratum, showing a single expanded tentacle crown with eight tentacles. D. Two campylonemidan tentacle crowns of zooids inside hole. E. Part of colony viewed from above to show stolon, kenozooids and zooids. Scale bar: E = 0.20 m.
FIGURE 15 in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 15. Bantariella verticillata (Heller, 1867), Cheongpodae, photographed live, specimen not preserved. A. Live colony on an intertidal stone. B. Campylonemidan tentacle crown with six tentacles forming a scoop shape and two angled away. C. Branching stolons and clusters of two to four zooids.
FIGURE 11 in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 11. Resin casts of Immergentia cheongpodensis n. sp. and Penetrantia taeanata n. sp. growing together at Cheongpodae. A. Resin cast showing mostly Penetrantia stolons and zooids, with those of Immergentia more apparent in the lower right quadrant. B. Close-up of crossing stolons, those of Penetrantia thicker and closer to the shell surface, with a broken zooid clearly with a peduncle, whereas the stolon of Immergentia runs across (beneath, in life orientation) a trifurcation in the Penetrantia colony. Scale bars: A = 0.50 mm; B = 0.10 mm.
FIGURE 6. Alcyonidium busanensis n in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 6. Alcyonidium busanensis n. sp., Namuseom Island, South Sea (MBRBKH6). A. Larvae being liberated from zooids. B. Ciliated larva. C–H. Compound-microscope images of living and preserved material. C. Cluster of developing embryos and larvae, removed from zooid. D. A ciliated larva and a developing embryo. E. Embryo magnified. F. Part of branch surface showing autozooids and kenozooids. G. Autozooids in partial side view showing small orifices. H. Retracted polypide. Scale bars: A = 4 mm; B = 0.60 mm; C–E = 0.20 mm; F = 0.44 mm; G = 0.30 mm; H = 0.14 mm.
FIGURE 18. Amathia medullaris Mawatari, 1972 in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 18. Amathia medullaris Mawatari, 1972 (MBRBK1708). A. Portion of a live colony encrusting the alga Stephanocystis hakodatense. B. Cluster of zooids, many containing yellow embryos. C. Another view of live colony on alga with expanded (10-tentacled) tentacle crowns. D. Closely spaced squat zooids, with developing embryos. E. View of growing tip of a colony, with zooids aligned on stolon, but not massively clustered as in older areas of colony. F. Compound-microscope view of retracted zooids showing walls of tubes and part of a setigerous collar. G. More-magnified view of two zooids, both brooding embryos. Scale bars: B, E = 0.30 mm; D = 0.13 mm; G = 0.15 mm.
FIGURE 5. Alcyonidium busanensis n in Korean ctenostome bryozoans-observations on living colonies, new records, five new species, and an updated checklist
FIGURE 5. Alcyonidium busanensis n. sp., Namuseom Island, South Sea (MBRBKH6). A. Live colony removed from fishing net. B. Another live colony showing branching pattern. C. Branch of live colony showing orange clusters of developing embryos inside some zooids. D. Colony surface showing zooid outlines, relatively small orifices, and clusters of embryos. Scale bars: A = 5 cm; C = 3 mm; D = 0.65 mm.
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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.