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Figures 2-14 from: Wei Y-W, Zhou Y-B, Zou Q-C, Sheng M-L (2020) A new species of Campoletis Förster (Hymenoptera, Ichneumonidae) with a key to species known from China, Japan and South Korea. ZooKeys 1004: 99-108. https://doi.org/10.3897/zookeys.1004.57913
Figures 2-14 Campoletis deserticola Sheng & Zhou, sp. nov. Holotype, female 2 habitus, lateral view 3 head, anterior view 4 clypeus and mandibles 5 head and pronotum, lateral view 6 mesoscutum and scutellum 7 mesosoma, lateral view 8 mesosoma, ventrolateral view 9 fore leg, lateral view 10 hind femur and tibia, lateral view 11 propodeum 12 first tergite, lateral view 13 postpetiole and tergites 2–4, dorsal view 14 ovipositor and ovipositor sheath, lateral view.
Figure 2 from: Wang G-T, Shu J-P, Jiang G-B, Chen Y-Q, Wang R-J (2021) Morphology and molecules support the new monotypic genus Fenghwaia (Rhamnaceae) from south China. PhytoKeys 171: 25-35. https://doi.org/10.3897/phytokeys.171.57277
Figure 2 Fenghwaia gardeniicarpa: A main stem with glabrous surface B young stem with pubescent surface C fertile branches D adaxial (left) and abaxial (right) side of leaf blade, respectively E serrated leaf margin F stipule G inflorescence H flower in anthesis I morphology of petals and stamens J longitudinal section of a flower, showing the stamens enclosed by cucullate petals K young fruit L transection section of an ovary, showing three ovules M mature fruit N transection section of mature fruit with only one well-developed seed O dehiscent capsule P seed, with an elongate and pronounced basal appendage. Photos: G.T. Wang, G.B. Jiang.
Figure 1 from: Wang G-T, Shu J-P, Jiang G-B, Chen Y-Q, Wang R-J (2021) Morphology and molecules support the new monotypic genus Fenghwaia (Rhamnaceae) from south China. PhytoKeys 171: 25-35. https://doi.org/10.3897/phytokeys.171.57277
Figure 1 The phylogenetic consensus tree of Rhamnaceae with ML and BI methods, on the basis of ITS and trnL-F sequences. AG: 'ampelozizyphoid' group. The numbers above the branches are Maximum Likelihood support values (left) and MrBayes posterior probability (right).
Supplementary Data of Microbial structures in the surface sediments of Shenhu Area, South China Sea
<p>Supplementary Data</p>
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: Speciation history of a species complex of Primulina eburnea (Gesneriaceae) from limestone karsts of south China, a biodiversity hotspot
Limestone karsts in southern China are characterized by high edaphic and topographic heterogeneity and host high levels of species richness and endemism. However, the evolutionary mechanisms for generating such biodiversity remain poorly understood. Here, we performed species delimitation, population genetic analyses, simulations of gene flow, and analyses of floral morphological traits to infer the geographic history of speciation in a species complex of Primulina eburnea from limestone karsts of south China. Using Bayesian species delimitation, we determined that there are seven distinct species that correspond well to the putative morphological species. Species-tree reconstruction, Structure and Neighbour-Net analyses all recovered four lineages in agreement with currently species geographic boundaries. High levels of genetic differentiation were observed both within and among species. Isolation–migration coalescent analysis provides evidence for significant but low gene flow among species. Approximate Bayesian computation (ABC) analysis supports a scenario of historical gene flow rather than recent contemporary gene flow for most species divergences. Finally, we found no evidence of divergent selection contributing to population differentiation of a suite of flower traits. These results support the prevalence of allopatric speciation and highlight the role of geographic isolation in the diversification process. At small geographic scales, limited hybridization occurred in the past between proximate populations but did not eliminate species boundaries. We conclude that limited gene flow might have been the predominant evolutionary force in promoting population differentiation and speciation.
FIGURE 4 in Revision of the Labeonine Genus Sinocrossocheilus (Teleostei: Cyprinidae) from South China
FIGURE 4. Map showing distributions of two species of Sinocrossocheilus in South China.
FIGURE 5 in Description of a new genus and two new species of labeonine fishes from South China (Teleostei: Cyprinidae)
FIGURE 5. Map showing distributions of two species of Hongshuia in South China.
FIGURE 4 in New data on soft corals (Cnidaria: Octocorallia: Alcyonacea) from Nha Trang Bay, South China Sea
FIGURE 4. Eleutherobia nezdoliyi sp. nov., holotype MIMB 16537, sclerites from the stalk interior.
FIGURE 3 in New data on soft corals (Cnidaria: Octocorallia: Alcyonacea) from Nha Trang Bay, South China Sea
FIGURE 3. Eleutherobia nezdoliyi sp. nov., holotype MIMB 16537, sclerites from the stalk surface.
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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.