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Figure 12 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 12 Cadophora prunicola sp. nov. A–G conidiophores and conidiogenous cells H conidia A–H from SNAA–HLM. Scale bar: 5 μm (A applies to B–H).
Figure 11 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 11 Cadophora obscuraA–J conidiophores and conidiogenous cells (arrows indicate short necks) K conidia A–K from SNAA–KLM. Scale bar: 5 μm (A applies to B–K).
Figure 10 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 10 Cadophora novi-eboraciA–G conidiophores and conidiogenous H conidia A–H from SNAA–HLM. Scale bar: 5 μm (A applies to B–H).
Figure 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
Figure 1 Phylogeny of dataset 1 obtained by Bayesian Inference analysis of the combined LSU and ITS sequence alignment for generic placement of strain GLMC 459. Geoglossum nigritum strain AFTOL-ID 56 is used as outgroup. BI posterior probability support values above 90% (bold) and ML and MP bootstrap support values above 70% are shown at the nodes. The strain, analysed in this study, is emphasised in bold. Green backgrounds indicate sequences included in the analyses of Han et al. (2014b). Blue backgrounds indicate close matches of GLMC 459 in blastn searches. Clades 1–10 of Hyaloscyphaceae, according to the analyses of Han et al. (2014b), are listed to the right. Family names are listed to the right, according to Han et al. (2014b, superscript H), Ekanayaka et al. (2019, superscript E) and Johnston et al. (2019, superscript J). Branches that are crossed by diagonal lines are shortened by 50%.
Figures 1-19 from: de Sousa VR, Pereira AFM, Couri MS (2020) On Aethiopomyia Malloch (Diptera, Muscidae) with the revision of the type specimens deposited in the Museum für Naturkunde, Berlin (Germany) with a key to species. ZooKeys 926: 73-80. https://doi.org/10.3897/zookeysw.926.49210
Figures 1-19 1–5Aethiopomyia arguta (Karsch, 1879) lectotype ♂ of Aricia arguta Karsch: 1 lateral view 2 dorsal view 3 head frontal view 4 pulvilli 5 labels 6–10Aethiopomyia gigas (Stein, 1906) syntype ♂: 6 lateral view 7 dorsal view 8 head frontal view 9 pulvilli 10 labels 11–14Aethiopomyia patersoni Zumpt, 1969 Paratype ♀: 11 lateral view; 12 dorsal view 13 head frontal view 14 labels 15–19Aethiopomyia williamsi (Snyder, 1951) ♀ of Lophomala anax Enderlein, 1927, nomen nudum: 15 lateral view 16 dorsal view 17 head frontal view 18 wing 19 labels. Scale bars: 5 mm (1–3, 5, 6–8, 10–19); 1 mm (4, 9).
Figures 20-30 from: de Sousa VR, Pereira AFM, Couri MS (2020) On Aethiopomyia Malloch (Diptera, Muscidae) with the revision of the type specimens deposited in the Museum für Naturkunde, Berlin (Germany) with a key to species. ZooKeys 926: 73-80. https://doi.org/10.3897/zookeysw.926.49210
Figures 20-30 Aethiopomyia arguta (Karsch, 1879) 20 aedeagus lateral view. Aethiopomyia gigas (Stein, 1906) 21 Sternite 5 22 cercal plate, lateral view 23 cercal plate, dorsal view 24 aedeagus dorsal view 25 aedeagus lateral view 26 ovipositor, dorsal view 27 ovipositor, ventral view 28 spermathecae 29 larva 30 detail of the anterior spiracle of larva. Scale bars: 0.2 mm 20–27, 29, 30; 0.1 mm 20, 28.
Fig. 7. Postcranium, Early Jurassic saurichthyids. A in Revision of Saurorhynchus (Actinopterygii: Saurichthyidae) from the Early Jurassic of England and Germany
Fig. 7. Postcranium, Early Jurassic saurichthyids. A. Saurorhynchus anningae sp. nov., neural arches and squamation in the posterior abdominal region (NHMUK PV P 3790). B–D. Saurorhynchus hauffi sp. nov., SMNS 55057. B. Lepidotrichia of the anal fin. C. Relationship between the neural and haemal arches and the axonosts. D. Caudal peduncle. Abbreviations: af.ax = axonosts of the anal fin; ax.p = axonost plate; bf = basal fulcra; cf.r = caudal fin radials; df.ax = axonosts of the dorsal fin; ff = fringing fulcra; hs = haemal spine; lep = lepidotrichia; mds = mid-dorsal scale row; mvs = mid-ventral scale row; na = neural arch; ns = neural spine. Scale bars: A = 1 mm, B–D = 5 mm. A. Photo © The Trustees of the Natural History Museum, London.
Model simulation data used in "Attributing ozone and its precursors to land transport emissions in Europe and Germany" (Mertens et al., ACP, 2020)
<p>This dataset contains the output of the MECO(n) regional model simulations analysed and discussed in Mertens et al. (ACP., 2020). An overview of the numerical experiments is given in the article. The README files in the dataset give additional information about the metadata.</p>
Figure 8 from: Steinbeck C, Koepler O, Bach F, Herres-Pawlis S, Jung N, Liermann JC, Neumann S, Razum M, Baldauf C, Biedermann F, Bocklitz TW, Boehm F, Broda F, Czodrowski P, Engel T, Hicks MG, Kast SM, Kettner C, Koch W, Lanza G, Link A, Mata RA, Nagel WE, Porzel A, Schlörer N, Schulze T, Weinig H-G, Wenzel W, Wessjohann LA, Wulle S (2020) NFDI4Chem - Towards a National Research Data Infrastructure for Chemistry in Germany. Research Ideas and Outcomes 6: e55852. https://doi.org/10.3897/rio.6.e55852
Figure 8 Components of TA2, Smart Lab, and connection to TA3: Seamless data transfer from devices via the ELN to repositories. Grey panels: modular software plugins, orange panels: modular software plugins for ELN and repositories, blue panels: software developed for the ELN. OC, IC, PC, PolyCC and AC represent the modules of the subdisciplines to be developed (see list of abbreviations in the last section of the Grant Proposal and the table to it).
Figure 7 from: Steinbeck C, Koepler O, Bach F, Herres-Pawlis S, Jung N, Liermann JC, Neumann S, Razum M, Baldauf C, Biedermann F, Bocklitz TW, Boehm F, Broda F, Czodrowski P, Engel T, Hicks MG, Kast SM, Kettner C, Koch W, Lanza G, Link A, Mata RA, Nagel WE, Porzel A, Schlörer N, Schulze T, Weinig H-G, Wenzel W, Wessjohann LA, Wulle S (2020) NFDI4Chem - Towards a National Research Data Infrastructure for Chemistry in Germany. Research Ideas and Outcomes 6: e55852. https://doi.org/10.3897/rio.6.e55852
Figure 7 Existing services forming the nucleus of the envisioned federation of repositories as part of the NFDI4Chem infrastructure.
Figure 11 from: Steinbeck C, Koepler O, Bach F, Herres-Pawlis S, Jung N, Liermann JC, Neumann S, Razum M, Baldauf C, Biedermann F, Bocklitz TW, Boehm F, Broda F, Czodrowski P, Engel T, Hicks MG, Kast SM, Kettner C, Koch W, Lanza G, Link A, Mata RA, Nagel WE, Porzel A, Schlörer N, Schulze T, Weinig H-G, Wenzel W, Wessjohann LA, Wulle S (2020) NFDI4Chem - Towards a National Research Data Infrastructure for Chemistry in Germany. Research Ideas and Outcomes 6: e55852. https://doi.org/10.3897/rio.6.e55852
Figure 11 TA6 will manage the synergies and interfaces to other NFDI consortia and the NFDI as a whole. It will ensure that cross-cutting topics such as NFDI-wide services are properly addressed and their results incorporated into NFDI4Chem.
Figure 10 from: Steinbeck C, Koepler O, Bach F, Herres-Pawlis S, Jung N, Liermann JC, Neumann S, Razum M, Baldauf C, Biedermann F, Bocklitz TW, Boehm F, Broda F, Czodrowski P, Engel T, Hicks MG, Kast SM, Kettner C, Koch W, Lanza G, Link A, Mata RA, Nagel WE, Porzel A, Schlörer N, Schulze T, Weinig H-G, Wenzel W, Wessjohann LA, Wulle S (2020) NFDI4Chem - Towards a National Research Data Infrastructure for Chemistry in Germany. Research Ideas and Outcomes 6: e55852. https://doi.org/10.3897/rio.6.e55852
Figure 10 The cultural change in chemical RDM is supported through training and community involvement in TA5 as well as by the NFDI4Chem infrastructure.
Germany and German Occupied Territories Imperial Prisoners of War Alphabetical List: Section 4: New Zealand: 2nd New Zealand Expeditionary Force
<p>CSV file of the members of the Second New Zealand Expeditionary Force that were taken prisoners of war in Germany and German Occupied Territories. This 1944 publication has been transcribed and matched against the Online Cenotaph database part of Auckland War Memorial Museum and includes 6370 entries. Most entries relate to Army personnel but it includes some Air Force prisoners of war. </p> <p>Includes reference to 56 Prisoner of War Camps.</p> <ul> <li>11A Altengrabow</li> <li>11B Fallingbostel</li> <li>13C Hammelburg am Main.</li> <li>17A Kaisersteinbruck nei Bruck (Leitha)</li> <li>17B Gneizendorf</li> <li>18A Wolfsber (Karnton)</li> <li>18A/Z Spitall/Drau.</li> <li>20A Thorn Podgorz.</li> <li>20B Marienburg</li> <li>21D Posen.</li> <li>2D Stagard.</li> <li>317 Markt Pongau (St. Johann)</li> <li>344 Lamsdorf</li> <li>357 Kopernikus</li> <li>383 Hohen Fels.</li> <li>398 Pupping near Ling</li> <li>3A Luckenwalde</li> <li>3B Furstenberg (R. Ode).</li> <li>3D Berlin-Steglitz</li> <li>4A Hohenstein</li> <li>4B Muhlberg (Elbe)</li> <li>4C Wistritz bei Teplitz</li> <li>4D Torgau (Elbe)</li> <li>4D/Z Annaburg</li> <li>4F Hartmandorf Chemnitz</li> <li>4G Oschatz</li> <li>5B Villingen Schwarzwald</li> <li>7A Moosburg (Isar)</li> <li>7B Memmingen</li> <li>8A Gorlitz</li> <li>8B Teschen</li> <li>8C Kunau Kzz Sprottau/Sagan</li> <li>9B Wegschelde</li> <li>9C Muhlhausen</li> <li>B.A.B. 20 Bau und Arbeits Battalion 20, Hydebreck</li> <li>B.A.B. 21 Bau und Arbeits Battalion 21, Blechammer</li> <li>Komaron</li> <li>Komarou</li> <li>L1 Stalag Luft 1, Barth Vogelsang</li> <li>L3 Stalag Luft 3, Sagan and Belaria</li> <li>L6 Stalag Luft 6, Heydekrug</li> <li>MUMN (Mar.) Marlag Nord, Westertimke (Tarnstedt)</li> <li>MUMN (Milag) Milag Nord, Westertimke (Tarnstedt)</li> <li>O.9A/H Spagenburg bei Kassel (O.9A/H)</li> <li>O.9A/Z Spagenburg bei Kassel (O.9A/Z)</li> <li>O12B Hadamar</li> <li>O4C Saalhaus Colditz</li> <li>O5A Weinberg (Wurtemburg)</li> <li>O79 Braunschweigh (formerly O.8F)</li> <li>O7B Eichstatt</li> <li>O9A/H Spagenburg bei Kassel</li> <li>O9A/Z Rotenburg Fulda</li> <li>O9B</li> <li>Siklos</li> <li>Slovakia</li> <li>Szigetva</li> </ul> <p>Original catalogue record can be found in <a href="https://www.aucklandmuseum.com/collections-research/collections/record/am_library-catalogq40-35824">Collections Online</a>.</p> <p> </p> <p>Field Names</p> <ul> <li><strong>Sequence number order</strong></li> <li><strong>Camp.No. P.O.W. No. Name Rank Army No.</strong> – original information</li> <li><strong>Camp.NO</strong> – Camp Number – split from original</li> <li><strong>POWNO</strong>. – Prisoner of War Number – split from original</li> <li><strong>Last name and initials</strong> – split from original</li> <li><strong>Rank</strong> – split from original</li> <li><strong>Army No.</strong> – split from original</li> <li><strong>Alias</strong> – split from original</li> <li><strong>Online Cenotaph number</strong> – Online Cenotaph system ID</li> <li><strong>Online Cenotaph Last name </strong>– Full name from Online Cenotaph</li> <li><strong>Online Cenotaph First names </strong>– Full first names from Online Cenotaph</li> </ul>
Desert-like badlands and surrounding (semi-)dry grasslands of Central Germany promote small-scale phenotypic and genetic differentiation in Thymus praecox
Environmental heterogeneity among sites can generate phenotypic and genetic variation facilitating differentiation and microevolution of plant populations. Badlands are desert-like, predominantly vegetation-poor habitats often embedded in (semi-)dry grasslands. The desert-like conditions of badlands demand extreme adaptation of plants, i.e., phenotypic modifications in short-term and/or natural adaptation in long-term. However, detailed knowledge is missing about both plant phenotypic and genetic differentiation in this unique and widely occurring habitat type. The present study focused on the largest known badlands systems in Central Europe located in the 'Drei Gleichen' region, a designated nature conservation area in Central Germany. Locations were suitable for this study in terms of having co-occurring badlands and (semi-)dry grassland habitats (sites) occupied by the pioneer plant Thymus praecox. Here, we studied the environmental preferences, morphological and functional trait variation, and genetic variation using microsatellite markers of T. praecox. Results revealed significant, mainly site-dependent environmental, phenotypic and genetic differentiation. In general, individuals in badlands are shorter in height, have lower patch sizes (length x width), relative growth rates, and smaller stomata. The PCA additionally unveiled slightly increased leaf robustness, trichome density, decreased stomatal conductance, fewer females, and earlier phenology in badlands. We interpret differentiation patterns as adaptive responses to light, temperature, drought and nutrient stress conditions supported by reviewed literature. Genetic differentiation was strongest between local badlands and grassland sites, and clearly weaker among locations and between sites (in total) as indicated by GST, AMOVA, PCoA and population structure. Our study supports the importance of small-scale microhabitat conditions as a driver of microevolutionary processes, and the population´s need for sufficient phenotypic plasticity and genetic resources to deal with environmental changes. We demonstrated that badlands are an appropriate model system for testing plant response to extreme habitats and that more research is needed on these fascinating landscapes.
FIGURE 5 in On the distribution and ecology of Culiseta (Culicella) ochroptera (Peus) (Diptera: Culicidae) in Germany
FIGURE 5. Variance of tergal scaling in female Culiseta ochroptera. A, Light form; B, dark form.
Figure 3 in New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany)
Figure 3. cf. Aeshna sp. (Aeshnidae), (A) photograph of specimen SMMG Ku 398 (Senckenberg Naturhistorische Sammlungen Dresden coll., Germany), imprint only; (B) line drawing of fore wing. Scale bars represent 5 mm.
Figure 1 in New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany)
Figure 1. Map of Cenozoic dragonfly localities in the Krušné hory piedmont basins and volcanic areas. Abbreviations: I, Cheb and Sokolov basins; II, Most Basin; III, České středohoří Mts. and Doupovské hory Mts.; 1, Želénky near Duchcov; 2, Bílina mine; 3, Kundratice near Litoměřice; 4, Seifhennersdorf; 5, Libouš mine; 6, Jehličná near Sokolov; 7, Marie Majerová mine near Sokolov; 8, Pochlovice near Kynšperk n. Ohří.
Figure 6 in New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany)
Figure 6.?Onychothemis rihai Prokop et al., 2003 (Libellulidae), (A) Photograph of specimen No. TN1 (Tomáš Novotný coll., Nástup Tušimice quarry, Czech Republic); (B) line drawing of fore wing. Scale bar represent 5 mm.
Figure 5 in New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany)
Figure 5.?Ictinogomphus species indet. (Lindeniidae), (A) Photograph of specimen under film layer of ethyl alcohol SMMG SaT 532 (Senckenberg Naturhistorische Sammlungen Dresden coll., Germany); (B) line drawing of fore wing. Scale bar represent 5 mm.
Figure 4 in New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany)
Figure 4. Genus and species indet. (Aeshnidae), (A) line drawing of fore wing; (B) photograph of specimen ZD 282 (Bílina Mine Enterprises, Bílina coll., Czech Republic). Scale bars represent 5 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.