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Figure 8 from: Chien-Ti C, Yen-Hsueh T (2019) Revision of Polygonatum (Asparagaceae, Nolinoideae, Polygonateae) of Taiwan. PhytoKeys 117: 99-118. https://doi.org/10.3897/phytokeys.117.31902
Figure 8 Polygonatumarisanensevar.formosanum. A habit B rhizome C leaf adaxial surface D leaf abaxial surface E inflorescences F flower G expanded perianth with stamens.
Figure 1 from: Kang G-W, Kolarov J, Lee J-W (2019) Cryptopimpla (Hymenoptera, Ichneumonidae, Banchinae) of South Korea, with description of two new species. ZooKeys 830: 99-109. https://doi.org/10.3897/zookeys.830.31974
Figure 1 Cryptopimplaaspeculosus sp. n. (holotype, male) A habitus in lateral view B head in frontal view C propodeum D first tergite in lateral view E wings. Scale bars: 2.0 mm (A); 0.2 mm (B, C); 0.5 mm (D); 1.0 mm (E).
Figure 4 from: Kang G-W, Kolarov J, Lee J-W (2019) Cryptopimpla (Hymenoptera, Ichneumonidae, Banchinae) of South Korea, with description of two new species. ZooKeys 830: 99-109. https://doi.org/10.3897/zookeys.830.31974
Figure 4 Cryptopimplapentagonalis sp. n. (female) A habitus in lateral view (holotype) B head in frontal view (holotype) C propodeum (holotype) D first tergite in lateral view (holotype) E wings (paratype). Scale bars: 2.0 mm (A); 0.5 mm (B, C, D); 1.0 mm (E).
Figure 3 from: Kang G-W, Kolarov J, Lee J-W (2019) Cryptopimpla (Hymenoptera, Ichneumonidae, Banchinae) of South Korea, with description of two new species. ZooKeys 830: 99-109. https://doi.org/10.3897/zookeys.830.31974
Figure 3 Cryptopimplacarinifacialis (male) A habitus in lateral view B head in frontal view C propodeum D first tergite in lateral view E wings. Scale bars: 2.0 mm (A); 0.5 mm (B,C, D); 1.0 mm (E).
Figure 2 from: Kang G-W, Kolarov J, Lee J-W (2019) Cryptopimpla (Hymenoptera, Ichneumonidae, Banchinae) of South Korea, with description of two new species. ZooKeys 830: 99-109. https://doi.org/10.3897/zookeys.830.31974
Figure 2 Cryptopimplabrevigena (male) A habitus in lateral view B head in frontal view C propodeum D first tergite in lateral view E wings. Scale bars: 2.0 mm (A); 0.2 mm (B, C); 0.5 mm (D); 1.0 mm (E).
FIGURE 99 in A new genus, Protaustrosimulium, for four species of Australian black flies (Diptera: Simuliidae)
FIGURE 99. Distribution of Protaustrosimulium. (99) Map of southern portion of Australia.
Figure 5 from: Zhang S-N, Hyde KD, Jones EBG, Jeewon R, Cheewangkoon R, Liu J-K (2019) Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99-129. https://doi.org/10.3897/mycokeys.49.30886
Figure 5 Longicorpusstriataspora (epitype MFLU 18–1580, epi-paratype MFLU 18–1582). a, b Appearance of ascoma on host surface c–e vertical section through an ascoma, with a clypeus near the ostiole f ostiole with periphyses g apex of the neck, with somewhat interwoven pale brown hyphae or setae h–k ascus l peridium in vertical section m vertical section of the neck, with thicker angular cells n pseudoparaphyses o–r ascospores s ascospore in India ink and presenting a clear mucilaginous sheath t germinating ascospore u, v Colony on PDA. Scale bars: 500 μm (a), 200 μm (b), 100 μm (c–e), 10 μm (f, l, n–t), 50 μm (g), 20 μm (h–k, m).
Figure 4 from: Zhang S-N, Hyde KD, Jones EBG, Jeewon R, Cheewangkoon R, Liu J-K (2019) Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99-129. https://doi.org/10.3897/mycokeys.49.30886
Figure 4 Striatiguttulaphoenicis (holotype MFLU 18–1579). a–c Appearance of ascoma on host surface d, e vertical section through an ascoma f ostiole g apex of the neck, with somewhat interwoven pale brown hyphae or setae h structure of peridium i, j pseudoparaphyses k–n asci o–t ascospores u ascospore in India ink and presenting a clear mucilaginous sheath v germinating ascospore w colony on PDA. Scale bars: 500 μm (a), 100 μm (b, c), 200 μm (d, e), 50 μm (f, g), 20 μm (h, k–n), 10 μm (i, j, o–v).
Figure 3 from: Zhang S-N, Hyde KD, Jones EBG, Jeewon R, Cheewangkoon R, Liu J-K (2019) Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99-129. https://doi.org/10.3897/mycokeys.49.30886
Figure 3 Striatiguttulanypae (holotype MFLU 18–1576, paratype MFLU 18–1578). a–c Appearance of stromata on host surface d–f vertical section through a stroma g structure of peridium h structure of clypeus near the ostiole, composed of epidermoidea cells and host tissue i ostiole with periphyses j pseudoparaphyses k apex of the neck, with somewhat interwoven pale brown hyphae or setae l–o ascus p–s ascospores t ascospore in India ink and presenting a clear mucilaginous sheath u germinating ascospore v colony on PDA. Scale bars: 500 μm (a), 200 μm (b, c), 100 μm (d–f), 10 μm (g, p–s, u), 20 μm (h, i, l–o, t), 50 μm (k).
Figure 1 from: Zhang S-N, Hyde KD, Jones EBG, Jeewon R, Cheewangkoon R, Liu J-K (2019) Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99-129. https://doi.org/10.3897/mycokeys.49.30886
Figure 1 RAxML tree of Pleosporales based on analysis of combined LSU, SSU, TEF1α and RPB2 sequence data. Bootstrap values for ML and MP equal to or greater than 75% are placed above and below the branches respectively. Branches with Bayesian posterior probabilities (PP) from MCMC analysis equal or greater than 0.95 are in bold. Newly generated sequences are indicated in red.
Figure 2 from: Zhang S-N, Hyde KD, Jones EBG, Jeewon R, Cheewangkoon R, Liu J-K (2019) Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99-129. https://doi.org/10.3897/mycokeys.49.30886
Figure 2 Maximum clade credibility (MCC) tree with divergence times estimates for Pleosporales and selected groups in Dothideomycetes, obtained from a Bayesian approach (BEAST) using one secondary and two fossil calibrations. Numbers at nodes indicate posterior probabilities (pp) for node support; bars correspond to the 95% highest posterior density (HPD) intervals. Numbers inside green circles indicate nodes used for calibrations: 1) the split of Arthoniomycetes and Dothideomycetes; 2) Metacapnodiaceae; 3) Margaretbarromycesdictyosporus.
Figure 99 from: Albano PG, Bakker PAJ, Sabelli B (2019) Annotated catalogue of the types of Triphoridae (Mollusca, Gastropoda) in the Natural History Museum of the United Kingdom, London. Zoosystematics and Evolution 95(1): 161-308. https://doi.org/10.3897/zse.95.32803
Figure 99 Viriolaalboguttata Tomlin, 1926, Scottburgh, Natal, South Africa. A–C, F–I Syntype NHMUK 1926.12.6.7: front (A, B), side (C), protoconch (F, G), aperture (H), peristome (I). D, E Original labels. Scale bars: A–C: 1 mm; F, G: 0.1 mm; H, I: 0.5 mm.
Figure 1 from: Karakehian JM, Quijada L, Friebes G, Tanney JB, Pfister DH (2019) Placement of Triblidiaceae in Rhytismatales and comments on unique ascospore morphologies in Leotiomycetes (Fungi, Ascomycota). MycoKeys 54: 99-133. https://doi.org/10.3897/mycokeys.54.35697
Figure 1 Morphological features of Triblidiaceae. a–d, h–l, uTriblidiumcaliciiformea dried apothecia on bark b same apothecia hydrated c 15 µm thick longitudinal section d dead asci containing living ascospores h–i ascospores j germinating ascospore k dead ascus containing living ascospores, detailing the apex l ascus detailing the apex (phl) u fine transverse striations of dehisced ascus (phl). e–g, m–tHuangshaniaverrucosae habit of apothecia on bark (dried) f detail of dried apothecia g detail of same apothecia hydrated m 15 µm thick longitudinal section in (Cr) n asci (KOH & Mlz) o detail of ascus apex (Cr) p ascospore q ascospore (cb/l) r detail of plug-like structure in a terminal cell of an ascospore s–t detail of verrucose ascospore surface (t in cb/l). All microphotographs of cells and tissues mounted in water unless otherwise noted: Congo red (Cr), cotton blue in lactophenol (cb/l), Melzer's reagent (Mlz), phloxine (phl), potassium hydroxide (KOH). † = dead, * = living. Scale bars: 1 mm (a–b, e–g); 50 µm (c, m–n); 20 µm (h–k, p–q); 10 µm (l, o); 5 µm (r–u). Specimens photographed: T.caliciiforme: a–b, d, j GJO-0088904; i FH-15071105; c, h, k–l, u CUP-18080101; H.verrucosa: UME-29336a.
Figure 4 from: Karakehian JM, Quijada L, Friebes G, Tanney JB, Pfister DH (2019) Placement of Triblidiaceae in Rhytismatales and comments on unique ascospore morphologies in Leotiomycetes (Fungi, Ascomycota). MycoKeys 54: 99-133. https://doi.org/10.3897/mycokeys.54.35697
Figure 4 Select examples of ascospore morphologies in Graphidaceae and Leotiomycetesa ascospores of Glyphiscicatricosa in Lugol's solution b muriform ascospore of Mellitiosporiumversicolorc–e muriform ascospores of Claussenomyces spp. within living, immature asci. All microphotographs of cells and tissues mounted in water unless otherwise noted. † = dead, * = living. Scale bars: 10 µm (a); 20 µm (b); 5 µm = (c–e). Specimens photographed: a = J.M.K personal collection; b = U.S.A., Oregon, Horse Rock Ridge, M. A. Sherwood, L. H. Pike & D. Wagner, 21 Mar 1979, FH [s.n.], image courtesy of Farlow Herbarium of Harvard University; c–e = L.Q. personal collections.
Figure 3 from: Karakehian JM, Quijada L, Friebes G, Tanney JB, Pfister DH (2019) Placement of Triblidiaceae in Rhytismatales and comments on unique ascospore morphologies in Leotiomycetes (Fungi, Ascomycota). MycoKeys 54: 99-133. https://doi.org/10.3897/mycokeys.54.35697
Figure 3 Bayesian majority-rule consensus tree of Leotiomycetes based on the ITS1-5.8S-ITS2 + LSU + mtSSU region. Thickened branches are those that were well supported by ML and BI methods. An asterisk indicates that this branch was supported only by Bayesian inference. Classification, orders and families follows Baral in Jaklitsch et al. (2016) using Trichoglossumhirsutum as the outgroup. Species for which molecular sequences have been generated for this study are given in bold followed by fungarium acronym, a dash, then identifying number.
Figure 2 from: Karakehian JM, Quijada L, Friebes G, Tanney JB, Pfister DH (2019) Placement of Triblidiaceae in Rhytismatales and comments on unique ascospore morphologies in Leotiomycetes (Fungi, Ascomycota). MycoKeys 54: 99-133. https://doi.org/10.3897/mycokeys.54.35697
Figure 2 Morphological features of Pseudographis. a–e, g, l–oPseudographispinicolaa dried apothecia on bark b same apothecia hydrated c–e hydrated apothecia g dead ascus containing living ascospores (cb), l ascospores m ascus containing mature ascospores, detail of apex (in dilute L) n ascospore emerging from ascus apex (Cr) o ascus apex. f, h–k, p–rPseudographiselatinaf hydrated ascomata h 15 µm thick longitudinal section i–j ascospores k ascospores (in dilute L) p detail of ascus apex (L) q turgid ascus r same ascus (in dilute L). All microphotographs of cells and tissues mounted in water unless otherwise noted: cresyl blue (cb), Congo red (Cr), Lugol's solution (L). † = dead, * = living. Scale bars: 1 mm (a–f); 50 µm (h, q–r); 20 µm (i–k); 10 µm (g, n–p); 5 µm (l–m). Specimens photographed: P.pinicola: a–b, g, l–o, FH-18061706; c–e courtesy of Adam Polhorský; P.elatina: GJO-0090016.
FIGURE 99 in Distribution, habitats, phenology and conservation of New Caledonian Odonata
FIGURE 99. Records of Rhyothemis phyllis apicalis.
Figure 2 from: Yang Q, Shi C, Ren D (2019) A new genus and species of berothids (Insecta, Neuroptera) from the Late Cretaceous Myanmar amber. ZooKeys 864: 99-109. https://doi.org/10.3897/zookeys.864.35271
Figure 2 Ansoberothajiewenae gen. et sp. nov., holotype CNU-NEU-MA2018072 A, B photograph of left forewing and line drawing C, D photograph of right forewing and line drawing E, F photograph of left hind wing and line drawing G, H photograph of right hind wing and line drawing. Scale bars 1 mm.
Figure 1 from: Yang Q, Shi C, Ren D (2019) A new genus and species of berothids (Insecta, Neuroptera) from the Late Cretaceous Myanmar amber. ZooKeys 864: 99-109. https://doi.org/10.3897/zookeys.864.35271
Figure 1 Ansoberothajiewenae gen. et sp. nov., holotype CNU-NEU-MA2018072 A photograph of holotype B detailed photograph of antenna, arrow shows the long scape C detailed photograph of abdomen, arrow shows the gonapophysis lateralis. Scale bars 2 mm (A) and 1 mm (B, C).
Figure 3 from: Hernández-Cárdenas RA, Serrato Díaz A, López-Ferrari AR, Espejo-Serna A (2019) Novelties in the genus Viridantha Espejo (Tillandsioideae, Bromeliaceae). PhytoKeys 132: 99-110. https://doi.org/10.3897/phytokeys.132.36959
Figure 3 Morphological comparison between Viridantha boqueronensis, V. penascoensis and V. uniflora Hern.-Cárdenas, Espejo & López-Ferr. V. unifloraA–B habit E–F, M spikes G plant with inflorescence H pistil I stamens J petals K sepals L floral bract (voucher: Hernández-Cárdenas et al. 2156, UAMIZ). V. boqueronensisC spike (voucher: K. and R. Ehlers EM7851, MEXU). V. penascoensisD spike (voucher: Hernández-Cárdenas and Sarabia 2116, UAMIZ). Photographs A–B by E. Negri Lavín; C–M by R. Hernández-Cárdenas.
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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)
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DANDI Archive for NWB datasets
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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.