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Figure 1 in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 1. Distribution of Plattenkalk basins and reef areas in the southern Franconian Alb during the Early Tithonian (slightly modified from Viohl, 1996). The new fish described herein was recovered in Ettling.
Figure 17 in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 17. Ascalabos voithii (neotype, JME SOS 537). Midcaudal vertebrae illustrating the presence of a lateral crest and grooves on the lateral side of the vertebral centra. Arrows point to a lateral longitudinal crest. Abbreviations: na, neural arch; ns, neural spine; ha, haemal arch; hs, haemal spine; vc, vertebral centrum.
Figure 14 in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 14. Ascalabos voithii (neotype, JME SOS 537). (a) Photograph of neotype in lateral view. Photograph courtesy of M. Ebert. Scale equals 1 cm. (b) Cranium in lateral view and enlargement of premaxilla (c). Abbreviations: ang, angular; cl, cleithrum; de, dentary; ent, entopterygoid; io1–3, infraorbitals 1–3; mx, maxilla; par, parasphenoid; pcl1, postcleithrum 1; pmx, premaxilla; pop, preopercle; ptt, posttemporal; qu, quadrate; scl, supracleithrum; scl.b, broken sclerotic bone; smx1–2, supramaxillae 1–2; sop, subopercle; sy, symplectic.
Figure 12. Ebertichthys ettlingensis n. gen. et n in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 12. Ebertichthys ettlingensis n. gen. et n. sp. Caudal fin and endoskeleton in lateral view (holotype JME ETT 108). Abbreviations: Ant, anterior; d.scu, dorsal caudal scute; ebfu, epaxial basal fulcra; ffu, fringing fulcra; H1–7, hypurals 1–7; hsPU4, haemal spine of preural centrum 4; nsPU2–4, neural spines of preural centra 2–4; naU1+2, neural arches of ural centrum 1 + 2; PH, parhypural; prp, procurrent rays; PU1, 4, preural centra 1, 4; U1+2, 3, ural centrum 1 + 2 and 3 (polyural terminology) fused with the bases of hypurals 1 and 2; 'UD', "urodermal"; UN1–4, uroneurals 1–4; PR1–19, principal rays 1–19; v.csu, ventral caudal scute.
Figure 7. Ebertichthys ettlingensis n. gen. et n in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 7. Ebertichthys ettlingensis n. gen. et n. sp. Dorsal and anal fins and their relationships to the vertebral column (JME ETT 132a). Abbreviations: Ant, anterior; an.r, principal anal rays; epl.b, epipleural bones; dor.r, dorsal principal rays; epin.p, epineural processes; ha, haemal arch; hs, haemal spine; la.pt, last anal pterygiophore; ld.pt, last dorsal pterygiophore; na, neural arch; ns, neural spine; paph, parapophyses; pr.anr, anal procurrent rays; pr.dr, dorsal procurrent rays; ri, ribs; sn, supraneural bones; V21, vertebra 21; 1st a.pt, first anal pterygiophore; 1st d.pt, first dorsal pterygiophore.
Figure 6. Ebertichthys ettlingensis n. gen. et n in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 6. Ebertichthys ettlingensis n. gen. et n. sp. Details of certain abdominal vertebrae and pectoral fin. (a) Anterior abdominal region and pectoral girdle and fin (holotype JME ETT 108). (b) Enlargement of a few abdominal vertebrae illustrating details of the epineural processes (holotype JME ETT 108). (c) Details of pectoral fin and radials (JME ETT 132a). Abbreviations: cl, cleithrum; cor, coracoid; d.ra, distal radials; epin.p, epineural process; na, neural arch; ns, neural spine; paph, parapophyses; pcl1–3, postcleithrum 1–3; pec.f, pectoral fin; pec.ra, proximal radials supporting pectoral rays; pel.p, pelvic plate; ptt, posttemporal; ri, ribs; sc, anterior field of cycloid scales; sca, scapula; scl, supracleithrum; sn, supraneurals; vc, abdominal vertebral centra; 1st. pec, first pectoral ray.
Figure 15 in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 15. Ascalabos voithii from Schernfeld in the Eichstätt Basin. Uncatalogued specimen from U. Eller (Dümpelfeld). (a) Photograph of specimen in lateral view. (b) Enlargement of the head. Note the peculiar shape and distribution of the sensory tubules of the preopercular canal. Photographs courtesy of U. Eller.
Figure 5. Ebertichthys ettlingensis n. gen. et n in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 5. Ebertichthys ettlingensis n. gen. et n. sp. Infraorbital bones, preopercle, suspensorium, and part of upper jaw (JME ETT 148). Abbreviations: hy, hyomandibula; io1–4, infraorbitals 1–4; io5?, broken infraorbital 5?; mtg, metapterygoid; mx, maxilla; pop, preopercle; qu, quadrate; smx1–2, supramaxillae 1–2.
Figure 20 in New remarkable Late Jurassic teleosts from southern Germany: Ascalaboidae n. fam., its content, morphology, and phylogenetic relationships
Figure 20. Hypothesis of phylogenetic relationships of the Late Jurassic Ascalabos and Ebertichthys n. gen. among the most primitive teleosts (highlighted in bold). Synapomorphies supporting the main nodes are listed below; for a complete list see Arratia (2013, 114– 118). Uniquely derived characters are identified with an asterisk [*]. See Supplement 1 for descriptions of characters listed below. Node A (teleosteomorphs or total-group teleost): 10[0]*, 24[1]*, 40[0]*, 47[2], 50[1], 94[0]*, 108[1], 112[1], 142[1]*, 164[1]*, 165[1]*, 168[1]*, and 169[1]*. Characters 142 and 164–168 are soft anatomical features that are unknown in fossils, but the parsimony analysis predicts that they were present at this phylogenetic level. Node B: 25[1], 34[1], 53[1], 55[1], 56[1], 59[1], 100[1], 109[1], 122[1], 125[1], and 162[1]. Node C: 47[1], 48[1], 59[2], 62[1], 63[1], 65[1], 69[1], 118[1], 148[2], and 153[1]. Node D: 78[1]*, 79[1], 102[1], 132[1], 150[1], and 151[1]. Node E: 13[1], 18[1], 56[0], 80[1]*, 96[1], 110[1], and 131[1]. Node F: 48[0], 66[1], 70[1], 82[1]*, 105[1], 108[0], 109[0], 127[1], and 129[1]. Node G: 3[1], 25[0], 42[1], 64[1], 68[1]*, 108[3], 111[1]*, and 162[0]. Node H: 28[1], 30[1], 32[1], 56[1], 67[1], 69[2], 83[1]*, 100[0], 103[1]*, 121[1], 124[1], 140[1], and 149[1]*. Character 103[1] was incorrectly listed as a synapomorphy of node E in Arratia (2013). Node I: 50[2], 107[1], 114[1], 119[1], 120[1], 144[1], 148[3], 152[1], 155[1], and 156[2]. Node J (Ascalaboidae, n. fam.): 25[1], 29[1]*, 30[2], 47[0], 49[1], 70[0], 97[1], 98[1]*, 99[1], and 145[1]. Node K: 86[1], 134[1], and 143[1]. Node L: 31[1], 33[1], 113[1], 116[1], 122[0], 141[1], and 146[1]. Node M: 36[1], 63[0], 65[0], 86[0], 104[1], 117[2], 132[3], 143[0], 136[1], 150[0], and 152[0]. Node M1: 25[0], 51[1], 56[0], 128[1], 133[1], 135[1], and 152[2]. Node M2: 31[0], 38[1], 41[1], 45[1], 49[2], 50[0], 59[1], 75[1], 91[1], 93[1], 112[0], 118[0], 123[0], 129[2], and 148[0].
Carbon sequestration potential in hedgerow soils: Results from 23 sites in Germany
<p>Dataset to the manuscript: Drexler, S. & Don, A. (2024). Carbon sequestration potential in hedgerow soils: Results from 23 sites in Germany. Geoderma. <a href="https://doi.org/10.1016/j.geoderma.2024.116878">https://doi.org/10.1016/j.geoderma.2024.116878</a></p> <ul> <li>Drexler_Don_2024_Data: contains the lab data for all samples</li> <li>Drexler_Don_2024_SOC_Stock_Per_Core: contains the calculated SOC stocks per soil core</li> </ul>
Fig. 4 in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 4 Cross-section of Aspidogaster limacoides, histology, from the level of the anterior edge of the ventral disc: A and D arrows (black and blue) showing marginal organs on ventral disc; B, E and F diagram of marginal organ (black and red arrows); C dorsoventral and longitudinal muscles (green arrows). Note: A–C H&E staining and D–F Alcian blue staining
Fig. 3 in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 3 Aspidogaster limcoides, SEM: A marginal organ with terminal duct (scale bar = 2 µm); B and B 2: Arrow showing pits inside the mouth (scale bar = 20 µm); C Ventral disc showing pits on alveoli and septa (scale bar = 10 µm); D dorsal view, posterior body with pits (scale bar = 2 µm); E excretory pore (scale bar = 20 µm)
Fig. 5 in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 5 Phylogenetic tree based on analyses of ITS1-5.8S-ITS2 sequences of species belonging to the genus Aspidogaster using the maximum likelihood method of phylogenetic reconstruction with TIM2 + I model according to jModelTest software v 2.1.10. Nodal numbers give bootstrap statistical support for the analyses. AN, Amur River, Nikolaevsk-na-Amure; AK, Amur River, Khabarovsk; Kh, Khanka Lake; Chi, China; ER, European part of Russia; Ger, Germany; JPN, Japan. *Misidentified A. chongqingensis
Fig. 2 in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 2 Aspidogaster limcoides, SEM: A dorsal view (scale bar = 100 µm); B ventral view with ventral disc (scale bar = 100 µm); C neck region, arrow showing depression of neck (scale bar = 20 µm), square D showing papillae-like structures posterior lateral to mouth; D posterior lateral papillae (arrow) (scale bar = 2 µm); E ventral disc, arrow showing marginal organ (scale bar = 20 µm); F ventral rim with marginal organ with terminal duct (arrow) (scale bar = 10 µm)
Fig. 1 Aspidogaster limacoides line drawings from Rutilus rutilus from North Germany. A in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 1 Aspidogaster limacoides line drawings from Rutilus rutilus from North Germany. A Dorsal view (scale bar = 500 µm); B ventral view (scale bar = 500 µm); C eggs (scale bar = 50 µm); D cirrus sac (scale bar = 200 µm)
Fig. 3 in Occurrence and regional distribution of Aelurostrongylus abstrusus in cats in Germany
Fig. 3 Seasonal distribution of Aelurostrongylus abstrusus-positive feline faecal samples (n 026) in Germany
Fig. 2 in Occurrence and regional distribution of Aelurostrongylus abstrusus in cats in Germany
Fig. 2 Light micrograph of a dehydrated, damaged and morphologically altered first-stage larva (L1) of Aelurostrongylus abstrusus after flotation using a concentrated salt solution with zinc chloride and sodium chloride (specific gravity, 1.3)
Fig. 1 in Occurrence and regional distribution of Aelurostrongylus abstrusus in cats in Germany
Fig. 1 Light micrograph of the posterior end of the first-stage larva (L1) of Aelurostrongylus abstrusus immobilised by heat
Fig. 13. Lamprobityle magnifica Heller, 1923 in Type specimens of the genera Doliops Waterhouse, 1841 and Lamprobityle Heller, 1923 (stat. nov.) (Coleoptera: Cerambycidae) and description of two new species deposited in Senckenberg Natural History collections Dresden, Germany
Fig. 13. Lamprobityle magnifica Heller, 1923 (=Doliops magnifica (Heller, 1923)) (A – dorsal view, B – lateral view, C – labels)
Fig. 1 Mosquito collections 2011–2019 in Nine years of mosquito monitoring in Germany, 2011-2019, with an updated inventory of German culicid species
Fig. 1 Mosquito collections 2011–2019 (green dots—trap collections; red dots— 'Mueckenatlas' submissions; blue dots—netting, aspirating and baited collections of adults; yellow dots—dipping/sieving of immature developmental stages)
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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.