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FIG. 11 in On unreported historical specimens of marine arthropods from the Solnhofen and Nusplingen Lithographic Limestones (Late Jurassic, Germany) housed at the Muséum national d'Histoire naturelle, Paris
FIG. 11. — Mesolimulus walchii (Desmarest, 1817):A, specimen MNHN.F.B13432; B, specimen MNHN.F.B13433. Scale bar: 1 cm. Photographs:L. Cazes.
FIG. 9. — A in On unreported historical specimens of marine arthropods from the Solnhofen and Nusplingen Lithographic Limestones (Late Jurassic, Germany) housed at the Muséum national d'Histoire naturelle, Paris
FIG. 9. — A, Cycleryon propinquus (Schlotheim, 1822): specimen MNHN.F.B13436 from Solnhofen; B-H, Eryon cuvieri Desmarest, 1817:B, specimen MNHN.F.A33501 from Solnhofen; C, specimen MNHN.GG.2004/8218 from Solnhofen area; this specimen was referred to as coming from Pappenheim; since there are no Solnhofen Lithographic Limestones there, while many traders lived there, this specimen was probably purchased in Pappenheim; D, E, specimen MNHN.GG.2004/8220 from Solnhofen, natural light (D) and UV light (E); F, G, specimen MNHN.F.A33545 from Solnhofen, natural light (F) and UV light (G); H, specimen MNHN.F.B13439 from unknown locality. Scale bars: A, C, F, H, 2 cm; B, D, E, F, 1 cm. Photographs: L. Cazes.
Antimicrobial resistance monitoring results complementing the EU Overview Summary Report on AMR in zoonotic and indicator bacteria from humans, animals and food in 2017/2018 - Germany
<p>This dataset contains AMR monitoring results in animals and food at the isolate level pursuant to Article 9 of Directive 2003/99/EC and to Annex, part B, of Commission implementing Decision 2013/652/EU. In addition, the dataset includes any other results from isolates than the ones mentioned in the Commission implementing Decision 2013/652/EU. The quantitative minimum inhibitory concentration (MIC) data from dilution methods are included. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: AMR_2018_DE_20200204: >> Federal Institute for Risk Assessment</p>
FIG. 3 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 3. — Specimen from Puech de la Suque, Montagne Noire, France (MN201): A, MN201-E2, general view showing several fragments of plants inside a partly decayed Clepsydropsis leclercqii Galtier, 1966 (Cl). A young Sphenophyllum stem (S) in transverse view is present at the bottom right; B, MN201-E2, general view of the Sphenophyllum stem on A showing the ribbed cortex (C) and the triangular stele with three protoxylem strands (arrows); C, MN201-E2, detail of the triangular stele; note the small lacunae in the best preserved protoxylem strand (arrow); D, MN201-E2, detail of the cortex; E, same specimen as A-D (MN201-F1) at another level, less well preserved but showing branching; F, same photo than E with the outline indicated in yellow, as well as the location of the primary xylem of the main axis (a) and of a lateral axis (b) also viewed in transverse section; the general outline of the cortex and oblique orientation of the tissue suggest the existence of another lateral organ towards the top of the photo (c); the tissues in the upper right corner correspond to part of the xylem of a Clepsydropsis Unger, 1856 rachis. Scale bars: A, 2 mm; B, E, 500 µm; C, D, 100 µm.
FIG. 4 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 4. — Specimen from Coumiac,Montagne Noire, France (MN911):A, slide MN911-A1,general view of the specimen above the level of branching,showing a main axis (a) on the left with a trace to a leaf (l) and a smaller axis (b) on the right;this section corresponds to the level 7 on Figure 7; B, slide MN911-A1,general view of the main axis in transverse section showing the cortex with six lobes and triangular primary xylem (arrows); C, slide MN911-A1,detail of the stele on A; note the presence of lacunae (arrow) at the extremity of each arm of the stele and the lack of secondary vascular tissues;D, slide MN911-A2,pitting on the primary xylem of an outgoing branch trace;E, slide MN911-A2, general view of the smaller axis shown on A; note smaller size of the primary xylem compared to B; F, slide MN911-A2,detail of the largest axis showing outgoing paired vascular traces at the extremity of the arm; G, slide MN911-A2, detail of F showing the protoxylem strand (arrow) and two outgoing traces (lt); H-K, successive sections showing the branching of the axis; H, below the division; I, node with leaves; J, branching; K, branching complete. These photos correspond to the levels 1, 2, 4, and 5 on Figure 7 and to polished surfaces MN911-B1i, MN911-B1s, MN911-B2s, and MN911-B3i. Scale bars: A, H-K, 1 mm; B, E, F, 200 µm; C, 80 µm; D, 50 µm.
FIG. 6 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 6. — Specimens with secondary growth from Kahlleite, Germany (KLC4 & KLC3): A, B, slides KLC4-A1 and KLC4-B1, general view of KLC4 in transverse sections at two different levels showing the triangular stele with three strands of protoxylem (arrows) and the outer cortex with 7 (A) or 6 (B) ridges; C, slide KLC4-B1, detail of the protostele in KLC 4 in transverse section showing a lacuna in at least one of the protoxylem locations; D, slide KLC4-B1, detail of the primary (X1) and secondary (X2) xylem in KLC4; note the files of secondary xylem tracheids separated by rays (arrows); E, slide KLC4-B1, detail of the outer cortex showing a decrease in cell diameter towards the outside of the stem (top of the image); F, slide KLC3-C, centre of KLC3 in a region where the center is preserved; arrows indicate the tip of the three arms of the actinostele; G, slide KLC3-C, detail of the protostele of KLC3 showing a primary xylem pole (arrow) and the development of secondary xylem (X2) around the primary xylem (X1); H, slide KLC3-C, detail of the secondary xylem in KLC 3 showing tracheids and rays (arrows) in transverse section. Scale bars: A, B, 500 µm; C, 200 µm; D, H, 50 µm; E, 20 µm; F, 250 µm; G, 100 µm.
FIG. 5 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 5. — Specimen with secondary growth from Puech de la Suque, Montagne Noire, France (MN864): A, slide MN864-C1, general view of the specimen in transverse section; the cortex is flattened but the central vascular tissues are not distorted; B, slide MN864-C1, central part of the axis in transverse section showing the cortex (C), the triangular shape of the primary xylem (X1), the position of the protoxylem (arrows), and a little development of secondary xylem (X2); a lacuna is present at the location of the protoxylem in the top right arm of the stele; C, slide MN864-C1, detail of secondary xylem (X2) in transverse section, with row of tracheids and possible ray cells (arrows); D, slide MN864-C1, more or less radial section through the stem showing the central part composed of primary and secondary xylem (X) and cortex (C); E, slide MN864-A5, detail of the box on element D showing possible tangentially elongated pits on the radial wall of secondary xylem tracheids; F, slide MN864-C1, detail of the cortex in transverse section showing a decrease in cell size and increase in wall thickness towards the periphery of the axis; G, slide MN864-A5, longitudinal section showing elongated cells of the cortex; H, slide MN864-A5, longitudinal section at a node showing the cortex (C) and a leaf base (l) cut obliquely; I, slide MN864-A5, detail of the leaf base on H; J, slide MN864-A6, longitudinal section at a node showing the cortex (C) and a leaf (l) showing its length and thickness. Scale bars: A, H, J, 500 µm; B, I, 200 µm; C, E-G, 50 µm; D, 250 µm.
Supplementary material 1 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
: Link: https://doi.org/10.3897/mycokeys.63.46836.suppl1
Figure 9 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 9 Cadophora luteo-olivacea. A–F conidiophores and conidiogenous cells (arrow indicates a short neck) G conidia A–G from SNAA–GLM. Scale bar: 5 μm (A applies to B–G).
Figure 6 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 6 Arboricolonus simplex gen. et sp. nov. A–J conidiogenous cells (arrows indicate conidiogenous openings or short necks) K conidia A–K from SNAA–KLM. Scale bar: 5 μm (A applies to B–K).
Figure 8 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 8 Cadophora bubakii comb. nov. A–H conidiophores and conidiogenous cells (arrows indicate short necks) I conidia A–I from SNAA–ILM. Scale bar: 5 μm (A applies to H–I).
Figure 7 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 7 Cadophora africana sp. nov. A–G conidiophores and conidiogenous cells (arrow indicates a short neck) H conidia A–H from SNAA–HLM. Scale bar: 5 μm (A applies to B–H).
Figure 5 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 5 Colony surface of analysed strains on OA medium. AArboricolonus simplexGLMC 459TBCadophora africanaCBS 120890TCC. bubakiiCBS 198.30TDC. luteo-olivaceaGLMC 1264 EC. novi-eboraciGLMC 1472 FC. obscuraCBS 269.33 GC. prunicolaCBS 120891THC. prunicolaGLMC 1633 IC. ramosaGLMC 377TJMinutiella pruni-aviumGLMC 1624TKProliferodiscus ingensGLMC 1751TLProliferodiscus sp. GLMC 460. Cultures A, J–L after 4 wk. Cultures B–I after 2 wk. Strains with a superscript T are ex-type cultures.
Figure 3 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 3 Phylogeny of dataset 3 obtained by Bayesian Inference analysis of the combined LSU, ITS, TUB sequence alignment of Phaeomoniellales, including Minutiella. Capronia fungicola strain CBS 614.96 is used as outgroup. BI posterior probability support values above 90% (bold), ML and MP bootstrap support values above 70% are shown at the nodes. The strains analysed in this study are emphasised in bold. Numbers of ex-type strains are emphasised with a superscript T. Branches that are crossed by diagonal lines are shortened by 50%.
Figure 4 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 4 Phylogeny of dataset 4 obtained by Bayesian Inference analysis of the combined LSU, ITS sequence alignment of Proliferodiscus and close relatives. Perrotia flammea strain JHH4497 is used as outgroup. BI posterior probability support values above 90% (bold), ML and MP bootstrap support values above 70% are shown at the nodes. The strains, analysed in this study, are emphasised in bold. Numbers of ex-type strains are emphasised with a superscript T.
Figure 2 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 2 Phylogeny of dataset 2 obtained by Bayesian Inference analysis of the combined ITS, TUB, EF-1α sequence alignment of Cadophora. Hyaloscypha finlandica strain CBS 444.86 is used as outgroup. Host plant or substrate and country of isolation are given for every strain. For strains isolated from Prunus spp. in Germany, the German Federal State is given in abbreviation as location. Species names are listed to the right. BI posterior probability support values above 90% (bold), ML and MP bootstrap support values above 70% are shown at the nodes. The strains, analysed in this study, are emphasised in bold. Numbers of ex-type and ex-isotype strains are emphasised with a superscript T. Branches that are crossed by diagonal lines are shortened by 50%. B: Bavaria; BW: Baden-Württemberg; LS: Lower Saxony; S: Saxony.
Figure 15 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 15 Proliferodiscus ingens sp. nov. A conidiomata B conidia formed in conidiomata C–E, H, I conidiogenous cells lining the inner wall of a conidioma F, G detached conidiogenous cells A–I from OAASMB–ILM. Scale bars: 300 μm (A), 5 μm (B applies to C–I).
Figure 16 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 16 Proliferodiscus sp. A conidiomata B conidia formed in conidiomata C–F, I–J conidiogenous cells lining the inner wall of a conidioma G, H detached conidiogenous cells H–J extensions on conidiogenous cells A–J from OAASMB–JLM. Scale bars: 300 μm (A), 5 μm (B applies to C–J).
Figure 14 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 14 Minutiella pruni-avium sp. nov. A, B conidiomata C–F conidiogenous cells lining the inner wall of a conidioma G conidia formed in conidiomata H–K, P–V conidiogenous cells formed on hyphal cells (arrows indicate conidiogenous openings) L–O mother cells W conidia formed on hyphal cells A–G from OAH–W from SNAA, BSM, C–WLM. Scale bars: 200 μm (A applies to B), 5 μm (C applies to D–W).
Figure 13 from: Bien S, Damm U (2020) Arboricolonus simplex gen. et sp. nov. and novelties in Cadophora, Minutiella and Proliferodiscus from Prunus wood in Germany. MycoKeys 63: 119-161. https://doi.org/10.3897/mycokeys.63.46836
Figure 13 Cadophora ramosa sp. nov. A–D conidiophores and conidiogenous cells E conidia A–E from SNAA–ELM. Scale bar: 5 μm (A applies to B–E).
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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.