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1,092 results for “The Sun”
Figure 8 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 8 Diaporthe melastomatis (SAUCC194.55) a branch with leaves of host plant b, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e, f conidiophores and conidiogenous cells g beta conidia h, i, k alpha conidia and beta conidia j alpha conidia. Scale bars: 10 μm (e–k).
Figure 7 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 7 Diaporthe lutescens (SAUCC194.36) a leaves of host plant b, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e–g conidiophores and conidiogenous cells h, i beta conidia. Scale bars: 10 μm (e–i).
Figure 5 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 5 Diaporthe heterostemmatis (SAUCC194.85) a leaf of host plant b, c surface (b) and reverse (c) sides of colony, after incubation for 15 days on PDAd conidiomata on PDAe, f conidiophores and conidiogenous cells g beta conidia h Alpha conidia i, j alpha conidia and beta conidia. Scale bars: 10 μm (e–j).
Figure 3 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 3 Diaporthe grandiflori (SAUCC194.84) a leaf of Heterostemma grandiflorumb, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e conidiophores and conidiogenous cells f alpha conidia g, i alpha conidia and beta conidia h beta conidia. Scale bars: 10 μm (e–i).
Figure 6 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 6 Diaporthe litchii (SAUCC194.22) a leaf of host plant b, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e, f conidiophores and conidiogenous cells g, h beta conidia i alpha conidia and beta conidia j alpha conidia. Scale bars: 10 μm (e–j).
Figure 11 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 11 Diaporthe tectonendophytica (SAUCC194.11) a leaf of host plant b, c surface (b) and reverse (c) side of colony after incubation for 15 days on PDAd conidiomata on PDAe, f conidiophores and conidiogenous cells g, h beta conidia. Scale bars: 10 μm (e–h).
Figure 2 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 2 Diaporthe camelliae-sinensis (SAUCC194.92) a leaf of host plant b, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e–h conidiophores and conidiogenous cells i beta conidia j–l alpha conidia and beta conidia m alpha conidia. Scale bars: 10 μm (e–m).
Figure 9 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 9 Diaporthe pungensis (SAUCC194.112) a leaf of host plant b, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata on PDAe–h conidiophores and conidiogenous cells i, l beta conidia j, k alpha conidia and beta conidia. Scale bars: 10 μm (e–l).
Figure 4 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 4 Diaporthe heliconiae (SAUCC194.77) a petiole of Heliconia metallicab, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata on PDAe–g conidiophores and conidiogenous cells h beta conidia i alpha conidia and beta conidia j alpha conidia k alpha conidia and germinating conidia. All in water. Scale bars: 10 μm (e–k).
Figure 1 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 1 Phylogram of Diaporthe based on combined ITS, TUB, TEF, CAL and HIS genes. The ML and BI bootstrap support values above 50% and 0.90 BYPP are shown at the first and second position, respectively. Strains marked with "*" are ex-type or ex-epitype. Strains from this study are shown in red. Three branches were shortened to fit the page size – these are indicated by symbol (//) with indication number showing how many times they are shortened.
Figure 10 from: Sun W, Huang S, Xia J, Zhang X, Li Z (2021) Morphological and molecular identification of Diaporthe species in south-western China, with description of eight new species. MycoKeys 77: 65-95. https://doi.org/10.3897/mycokeys.77.59852
Figure 10 Diaporthe subclavata (SAUCC194.66) a leaf of Pometia pinnatab, c surface (b) and reverse (c) sides of colony after incubation for 15 days on PDAd conidiomata e–h conidiophores and conidiogenous cells i, j Beta conidia k, l Alpha conidia. Scale bars: 10 μm (e–l).
Data from: Gliding lizards use the position of the sun to enhance social display
Effective communication requires animal signals to be readily detected by receivers in the environments in which they are typically given. Certain light conditions enhance the visibility of colour signals and these conditions can vary depending on the orientation of the sun and the position of the signaller. We tested whether Draco sumatranus gliding lizards modified their position relative to the sun to enhance the conspicuousness of their throat-fan (dewlap) during social display to conspecifics. The dewlap was translucent, and we found that lizards were significantly more likely to orient themselves perpendicular to the sun when displaying. This increases the dewlap's radiance, and likely, its conspicuousness, by increasing the amount of light transmitted through the ornament. This is a rare example of a behavioural adaptation for enhancing the visibility of an ornament to distant receivers.
Data from: Orientation to the sun by animals and its interaction with crypsis
1. Orientation with respect to the sun has been observed in a wide range of species and has generally been interpreted in terms of thermoregulation and/or ultraviolet (UV) protection. For countershaded animals, orientation with respect to the sun may also result from the pressure to exploit the gradient of coloration optimally to enhance crypsis. 2. Here, we use computational modelling to predict the optimal countershading pattern for an oriented body. We assess how camouflage performance declines as orientation varies using a computational model that incorporates realistic lighting environments. 3. Once an optimal countershading pattern for crypsis has been chosen, we determine separately how UV protection/irradiation and solar thermal inflow fluctuate with orientation. 4. We show that body orientations that could optimally use countershading to enhance crypsis are very similar to those that allow optimal solar heat inflow and UV protection. 5. Our findings suggest that crypsis has been overlooked as a selective pressure on orientation and that new experiments should be designed to tease apart the respective roles of these different selective pressures. We propose potential experiments that could achieve this.
FIGURE 4 in A new species of sun-spider from sand dunes in Coahuila, Mexico, (Arachnida: Solifugae: Eremobatidae)
FIGURE 4. Eremocosta arenarum sp. nov. Sternites X–XII of males showing ctenidia
FIGURE 7 in A new species of sun-spider from sand dunes in Coahuila, Mexico, (Arachnida: Solifugae: Eremobatidae)
FIGURE 7. Landscape in the type locality (Photograph by Kari J. McWest).
FIGURE 27. Mummucia ibirapemussu n in A new species of the sun-spider genus Mummucia (Arachnida: Solifugae: Mummucidae) from Piauí, northeastern Brazil
FIGURE 27. Mummucia ibirapemussu n. sp., habitus of preserved adult male, dorsal view.
Supplementary material 1 from: Mei Z, Sha Z, Sun S (2023) Going deeper and further: a range and depth extension for the deep-sea feather star Paratelecrinus cubensis (Carpenter, 1881) (Comatulida, Atelecrinidae), first record from the Western Pacific. ZooKeys 1184: 103-113. https://doi.org/10.3897/zookeys.1184.110577
Sequence information needed to construct phylogenetic trees
Supplementary material 1 from: Guo X, Liu X-Y, Jiang S-Y, Guo S-X, Wang J-F, Hu Y, Li S-M, Li H-M, Wang T, Sun Y-K, Li M-Y (2023) Allelopathy and arbuscular mycorrhizal fungi interactions shape plant invasion outcomes. NeoBiota 89: 187-207. https://doi.org/10.3897/neobiota.89.110737
Responses of the aboveground biomass of native plant species to the allelopathy (n = 10)
Figure 2 from: Huang S, Xia J, Zhang X, Sun W (2021) Morphological and phylogenetic analyses reveal three new species of Diaporthe from Yunnan, China. MycoKeys 78: 49-77. https://doi.org/10.3897/mycokeys.78.60878
Figure 2 Diaporthe arecae (SAUCC194.18) a infected leaf of Persea americanab, c surface and reverse of a colony after 15 days on PDAd conidiomata e–g conidiophores and conidiogenous cells h beta conidia i alpha conidia j alpha conidia and beta conidia. Scale bars: 10 μm (e–j).
Figure 3 from: Gu X, Wang R, Sun Q, Wu B, Sun J-Z (2020) Four new species of Trichoderma in the Harzianum clade from northern China. MycoKeys 73: 109-132. https://doi.org/10.3897/mycokeys.73.51424
Figure 3 Trichoderma vermifimicola (CGMCC 3.19694). Cultures at 25 °C after 3 days (A on PDA B on CMDC on SNA) D conidiation pustules on CMD after 10 days E conidiation pustules on SNA after 10 d F, H conidiophores G, J, K conidiophores and phialides I conidia. Scale bars: 25 µm (F, H); 10 µm (G, J–K).
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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.