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1,140 results for “Colony”
FIGURE 5. Graptopetalum kristenii. A. Colony showing various rosettes with inflorescence. B in Graptopetalum kristenii (subg. Glassia, Crassulaceae), a new haplostemonous species from Michoacán, Mexico
FIGURE 5. Graptopetalum kristenii. A. Colony showing various rosettes with inflorescence. B. Comparison between leaves and flowers of G. kristenii (left) and G. pentandrum (right). C–D. Flowers with different petal color patterns. E. Comparison between rosettes of G. kristenii and G. pentandrum. F. Branch segment with flowers and buds. G. Flower with measurements (mm). H. Leaf with measurements (mm). Photographs by J. Etter and M. Kristen.
FIGURE 8 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 8. Dorsal views of hypopygia. A–D Larva living in Nostoc. B, C adapted from Willis W. Wirth (1957). D adapted from Ashe & Murray (1980). E, F adapted from Sasa M. & Kikuchi M. (1995). Bars: 50 µm.
FIGURE 7 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 7. Left two drawings: a tunnel made by Cricotopus nostocicola in a spherical colony of the cyanobacteria Nostoc parmelioides from Brock (1960). Right picture: Nostoc colony with larva found at Ashiu, Japan.
FIGURE 6. 3D in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 6. 3D computer tomography scan images of Nostoc colony with larva. The white dashed line encloses the larva.
FIGURE 1. A in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 1. A map of the collection sites (S1–S3) of Nostoc colonies symbiotic with chironomids. Information on the sites is listed in Table 1.
FIGURE 5 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 5. Cricotopus cataractaenostocicola sp. nov., larva and pupa. Larva (A–G), A and A': general appearance, B: dorsal view of head capsule, C: frontal view of head, D: larval left antenna, E: top of the head, F: anterior parapods, G: posterior parapods. Pupa, H, H' and H": general appearance. H' is a combination of three pictures, two dotted lines are borders. I: tergite IV from the side, J: tergite VII from the side, K: face. Photos C–F, H' and K were obtained by an electronic microscope. Abbreviations (larva). Ap: anterior parapods; As: anal seta; Pp: posterior parapods; Ta: anal tubules. Abbreviations (pupa). Al: anal lobe.
FIGURE 2 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 2. Landscapes of the habitats of the Nostoc colonies symbiotic with chironomids. Information on the sites is listed in Table 1.
FIGURE 4 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 4. Cricotopus cataractaenostocicola sp. nov. Adult male (A–G'), A: general appearance, B: antenna, C: thorax, D: hypopygium, E: eye, F: thorax and head, G, G', and G": right wing. Adult female (H–L), H and H': general appearance, I: head, J and J': genitalia, K: antenna. Abbreviations (adult). Al: alula; An: anal vein; Ap: anal point; Ce: cercus; Clw: craw, Cp: cibarial pump; Dc: dorsocentrals; Gc: gonocoxite; Gs: gonostylus; Hl: halter; Ivo: inferior volsella; La: labrum; Pm: palpal segments; Po: Postnotum; Sct: scutelium; Scu: scutum; Sq: squama.
FIGURE 3 in A new species, Cricotopus cataractaenostocicola, living in a cyanobacterial colony on vertical rocky substrates with trickling water film in Japan (Diptera: Chironomidae)
FIGURE 3. Phylogeny based on the COI dataset. Information on the sequences used for this analysis is shown in Table 2.
FIGURE. Cladosporium benschii (VIC 44412, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–J. Non-geniculate macronematous conidiophores and conidia. K. Conidiogenous cells with slightly protuberant loci. L. Micronematous conidiophores. M. Microcyclic conidiogenesis. Scale bars: E–M = 20 µM. in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. Cladosporium benschii (VIC 44412, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–J. Non-geniculate macronematous conidiophores and conidia. K. Conidiogenous cells with slightly protuberant loci. L. Micronematous conidiophores. M. Microcyclic conidiogenesis. Scale bars: E–M = 20 µM.
FIGURE. Cladosporium bambusicola (VIC 44237, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–F. Conidiophore and bigger conidia. G–H. Conidiophores and smaller conidia. I. Stromatic hyphal aggregation. J–K. Micronematous conidiophores. L. Ramoconidia and conidia. M. Microcyclic conidiogenesis. Scale bars: E = 50 µM; F–M = 20 µM. in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. Cladosporium bambusicola (VIC 44237, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–F. Conidiophore and bigger conidia. G–H. Conidiophores and smaller conidia. I. Stromatic hyphal aggregation. J–K. Micronematous conidiophores. L. Ramoconidia and conidia. M. Microcyclic conidiogenesis. Scale bars: E = 50 µM; F–M = 20 µM.
FIGURE. Cladosporium aulonemiae (VIC 44413, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–G. Macronematous conidiophores and numerous conidia; H–I. Formation of loci in close succession; I. Spread polysaccharide-like material; J. Micronematous conidiophores; K. Ramoconidia and conidia; L. Microcyclic conidiogenesis; M. Stromatic hyphal aggregation. Scale bars: E–M = 20 µM. in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. Cladosporium aulonemiae (VIC 44413, holotype). A–D. Colonies on A. Potato dextrose agar; B. Malt extract agar; C. Oatmeal agar; D. Synthetic nutrient-poor agar, after 14 days at 25 ºC, under near-ultraviolet light, respectively. E–G. Macronematous conidiophores and numerous conidia; H–I. Formation of loci in close succession; I. Spread polysaccharide-like material; J. Micronematous conidiophores; K. Ramoconidia and conidia; L. Microcyclic conidiogenesis; M. Stromatic hyphal aggregation. Scale bars: E–M = 20 µM.
FIGURE. Dothiorella viticola on dead branch of Morus sp. (MFLU 19-0621). a, b. Conidiomata on host substrate. c. Vertical section through conidioma. d. Ostiole. e. Peridium of conidioma. f–j. Conidia attached to conidiogenous cells. k–m. Conidia. n. Germinating conidium. o, p. Colony on PDA (o upper, p lower). Scale bars: a = 1 mm, b = 100 μm, c = 50 μm, d = 20 μm, e–n = 10 μm. in Two new species of Botryosphaeriaceae (Botryosphaeriales) and new host/ geographical records
FIGURE. Dothiorella viticola on dead branch of Morus sp. (MFLU 19-0621). a, b. Conidiomata on host substrate. c. Vertical section through conidioma. d. Ostiole. e. Peridium of conidioma. f–j. Conidia attached to conidiogenous cells. k–m. Conidia. n. Germinating conidium. o, p. Colony on PDA (o upper, p lower). Scale bars: a = 1 mm, b = 100 μm, c = 50 μm, d = 20 μm, e–n = 10 μm.
Data from: Variation in male-built nest volume with nesting-support quality, colony and egg production in whiskered terns
<p class="Standard"><span>Nest building can represent an energetically-costly activity for a variety of animal taxa. Besides, the determinants of within-species variation in the design of nests, notably with respect to natural and sexual selection, are still insufficiently documented. Based on an observational study, we examined the influence of nesting conditions (nesting-support quality, colony, laying date, and year) on male-built nest volume and also its potential role as a post-mating sexually-selected display in the whiskered tern <i>Chlidonias hybrida</i>. This tern species is a monogamous colonial bird with obligate bi-parental care breeding on aquatic vegetation. Hence, large nesting platforms are expected to be a selective advantage because they would better withstand adverse environmental conditions and provide a secure structure for eggs. Nest size may also serve as a post-mating sexual trait, and variation in egg production would be positively associated to nest size. We found that nest volume was adjusted to different environmental cues. A positive relationship was found between nest volume and nesting-support quality indicating that the leaf density of white waterlily is essential for nest stability. Variation in nest volume was not correlated to colony size but varied among colonies and years. Male-built nest volume was also positively associated with mean egg volume per clutch but not with clutch size. The fitness consequences of building a large nest are yet to be studied, and, additional investigations are recommended to better understand whether the activity of males early during breeding season (e.g. nest building and courtship feeding performance) really serves as post-mating sexually-selected signals.</span></p>
Continuous exchange of nectar nutrients in an Oriental hornet colony- Dataset
<p>Raw data of the experiments " Continuous exchange of nectar nutrients in an Oriental hornet colony".</p>
Dataset of PNAS article "Morphological instability and roughening of growing 3D bacterial colonies"
<p>Dataset of the PNAS article "Morphological instability and roughening of growing 3D bacterial colonies", including numerical simulations and raw images of all Main Text and SI figures.</p>
Dataset with values of morphological parameters and phenotypes of cells and colonies from three human pluripotent stem cell lines
<p>The dataset is a part of the following manuscript submitted for publication in International Journal of Molecular Sciences (MDPI):</p> <p>"Prognostic Analysis of Human Pluripotent Stem Cells Based on their Morphological Portrait and Expression of Pluripotent Markers" by Olga A. Krasnova, Vitaly V. Gursky, Alina S. Chabina, K. A. Kulakova, L. L. Alekseenko, Alexandra V. Panova, Sergey L. Kiselev and Irina E. Neganova</p> <p>The files contain values of several morphological parameters and phenotypes obtained for cells and colonies from hESC line H9, hiPSC line AD3, and hiPSC line CaSR. The phenotypic information is presented in three forms: four possible classes of colonies according to the visually assessed phenotype ('bad', 'average', 'good', and 'excellent'), three possible classes (previous 'good' and 'excellent' combined in one 'good' class), and two possible classes (previous 'bad' and 'average' combined in one 'bad' class, and previous 'good' and 'excellent' combined in one 'good' class).</p>
Fachada Colonial
Source: Objaverse 1.0 / Sketchfab
Kero estilo colonial
Source: Objaverse 1.0 / Sketchfab
Lazzaretti Colony, Monte Labbro, Arcidosso Italy
The ruins of the hermitage, the Torre Davidica or Torre Giurisdavidica, of David Lazzaretti or Davide Lazzaretti (Arcidosso, November 6, 1834 - Bagnore, August 18, 1878), an Italian preacher and rebel. His name is linked to the Giurisdavidismo, his doctrine.Monte Labbro, Arcidosso, Grosseto, Tuscany, Italy. He worked in Tuscany in the Monte Amiata region at the end of the nineteenth century. For his visionary vision and his tragic end he was called the Christ of Amiata or the Prophet of Amiata. The aversion of the state and the church to his messianism caused his death, which took place on August 18, 1878, when he was killed by the Carabinieri at the end of an impressive parade in Arcidosso. The Mt. Amiata Project is an ongoing GDH collaboration involving faculty and students at the University of Florence and the University of Siena. We could not have done this project without the considerable support of the Municipality of Arcidosso. 5675 Drone and Terrestrial photos, 61 Faro laser scans Source: Objaverse 1.0 / Sketchfab
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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.