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Fig. 11. Neighbour-joining tree showing p in Two new species of Leptanilloides Mann, 1823 (Formicidae: Dorylinae) from the Andes of southern Ecuador
Fig. 11. Neighbour-joining tree showing p-distances among DNA sequences of the mitochondrial COI barcode fragment obtained for all specimens of Leptanilloides Mann, 1823 sequenced here and available in GenBank and BOLD. The tree was rooted with a COI sequence of Cylindromyrmex striatus Mayr, 1870 (GenBank accession number AY233723). Labels provide species identifications and field IDs (in bold) or GenBank or BOLD numbers. Values at nodes indicate bootstrap support only if it was above 80%.
Figures 78-79. Theridion spinitarse O. P in Notes on Mediterranean Theridiidae (Araneae) – II
Figures 78-79. Theridion spinitarse O. P.-Cambridge. Epigynum/vulva, ventral (78), dorsal view (79), drawn at same scale. Scale line: 0.10 mm.
Figures 19-22. D. shardana holotype, right male bulb 19 prolateral view, general 20 prolateral view, tip detail 21 anterior view 22 P in Systematics and phylogeography of the Dysdera erythrina species complex (Araneae, Dysderidae) in Sardinia
Figures 19-22. D. shardana holotype, right male bulb 19 prolateral view, general 20 prolateral view, tip detail 21 anterior view 22 P, prolateral view.
Figures 6-10. 6. P in Revision of the "Aemilia" ambigua (Strecker) species-group (Noctuidae, Arctiinae)
Figures 6-10. 6. P. ambigua, right lateral view of male genital capsule, aedeagus removed. 7. P. syracosia, lateral view of right valve. 8. P. fallaciosa, lateral view of right valve. 9. P. sonorosa, lateral view of right valve. 10. P. potosi, lateral view of right valve.
Figures 1-5. 1a. P in Revision of the "Aemilia" ambigua (Strecker) species-group (Noctuidae, Arctiinae)
Figures 1-5. 1a. P. ambigua male (Santa Cruz Co., AZ, USA). 1b. P. ambigua female (Cochise Co., AZ, USA). 2a. P. syracosia male (Zacapa Dpto., Guatemala). 2b. P. syracosia female (Chiapas, Mexico). 3a. P. fallaciosa male (Chiapas, Mexico). 3b. P. fallaciosa female (Zacapa Dpto., Guatemala). 4a. P. sonorosa male paratype (Sonora, Mexico). 4b. P. sonorosa female paratype (Sonora, Mexico). 5. P. potosi male holotype (Nuevo Leon, Mexico).
Hilbert-P\'{o}lya conjecture and Riemann hypothesis
<p>Since Hilbert-P\'{o}lya conjecture has been solved by the G-dynamics ${{\widehat{w}}^{\left( cl \right)}}$ as a Hermitian frequency operator, the Riemann hypothesis as a corollary of Hilbert-P\'{o}lya theorem is proven as well, then we have explicitly asserted the physical essence of Riemann hypothesis expressed by $$\zeta \left( \rho \right)=\zeta \left( \varrho/\hbar \right)=0$$ where the non-trivial zeros $\rho =1/2+\sqrt{-1}{{w}^{\left( q \right)}}$. Furthermore, we have geometrically proven Einstein tensor such that ${{G}_{ij}}=\zeta \left( \rho\right)=0$, and ${w}^{\left( q \right)}=R$ is the scalar curvature.</p>
Figs 1-16 in Notes on the genus Psychonotis (Lepidoptera: Lycaenidae) from Western New Guinea (Papua and Papua Barat), with description of a new subspecies of P. melane (Joicey & Talbot, 1916)
Figs 1-16. Psychonotis caelius plateni (Grose-Smith & Kirby, 1896) [all in CSSK]. Fig. 1. ♂, upperside, Waigeo, no date; Fig. 2. underside; Fig. 2a. Hindwing showing the green metallic lunules and white marginal streaks; Fig. 3. ♂, upperside, Waigeo, x.2009; Fig. 4. underside; Fig. 5. ♂, upperside, Nabire, Kaladiri vill., xii.2013; Fig. 6. underside; Fig. 7. ♀, upperside, Sorong, i.2012; Fig. 8. underside; Fig. 9. ♀, upperside, Timika, vi.2001; Fig. 10. underside; Fig. 10a. Hindwing with reduced marginal streaks; Fig. 11. ♀, upperside, Yapen, Ambaidiru, iii.2006; Fig. 12. underside; Fig. 13. ♂, upperside, Bulolo, vi.2001; Fig. 14. underside; Fig. 15. ♂, upperside, Madang, Tokan vill., vi.2001; Fig. 16a. Hindwing with well developed marginal streaks. [scale for set specimens = 1cm]
Figs 17-22 in Notes on the genus Psychonotis (Lepidoptera: Lycaenidae) from Western New Guinea (Papua and Papua Barat), with description of a new subspecies of P. melane (Joicey & Talbot, 1916)
Figs 17-22. Psychonotis caelius cf. plateni (Grose-Smith & Kirby, 1896). Fig. 17. ♂, upperside, Arfak Mountains., ix.2013, CSSK; Fig. 18. underside; Fig. 19. ♀, upperside, Arfak Mountains., Duebei, 1200m, i.2011, CSSK; Fig. 20. underside; Fig. 21. ♂, upperside, Peg. Bintang, Batimban, Dau River, vii.2003, KSP12091; Fig. 22. Underside; Fig. 23. Psychonotis caelius dissimilis (Joicey & Talbot, 1916), ♂ upperside, Supiori Isl., viii.-ix.2006, CSSK; Fig. 24. underside; Fig. 25. Psychonotis eudocia Druce & Bethune-Baker, 1893, ♂, upperside, Bacan, Labuha, ix.2015, CSSK; Fig. 26. Underside (note the short yellowish streak at the forewing base); Fig. 27. Psychonotis melane melane (Joicey & Talbot, 1916), ♂, upperside, Wissel Lake, Tuguwai, xii.1980, KSP11926; Fig. 28. underside; Fig. 29. Psychonotis melane astra subsp. nov., ♂, paratype, upperside, Star Mountains, Peg. Bintang, Mabilabol, ii.2005, KSP 11928; Fig. 30. underside; Fig. 31. Psychonotis melane astra subsp. nov., ♂, holotype, upperside, Star Mountains, Peg. Bintang, Mabilabol, ii.2005, KSP11930; Fig. 32. underside; Fig. 33. Psychonotis melane melane (Joicey & Talbot, 1916), ♂, left valva, KSP11924. Fig. 34. Psychonotis melane astra subsp. nov., ♂, left valva (note the more rectangular outline and the slightly stronger teeth), KSP11928. [scale for set specimens = 1cm]
Fig. 3 in Description of five new species in the genus Phlyctinus Schoenherr (Coleoptera, Curculionidae): a first step in deciphering the P. callosus complex
Fig. 3 (opposite page). A–B. Ventrites of males of Phlyctinus Schoenherr, 1826 (left: ventrites 1–5, right: ventrite 5). A. P. callosus (Schoenherr, 1826). B. P. grootbosensis Haran sp. nov. C–D. Ventrite 5. C. P. xerophilus Haran sp. nov., holotype ♂. D. P. planithorax Haran sp. nov. E–F. Vestiture of basal right side of elytra. E. P. callosus (Schoenherr, 1826) (left). F. P. littoralis Haran sp. nov. Scale bars = 0.5 mm.
Fig. 2 in Description of five new species in the genus Phlyctinus Schoenherr (Coleoptera, Curculionidae): a first step in deciphering the P. callosus complex
Fig. 2. Penis of Phlyctinus Schoenherr, 1826, in dorsal (left) and lateral (right) view, and copulatory sclerite (top right). A. P. callosus (Schoenherr, 1826). B. P. grootbosensis Haran sp. nov. C. P. xerophilus Haran sp. nov., holotype ♂. D. P. planithorax Haran sp. nov., holotype ♂. E. P. littoralis Haran sp. nov., holotype ♂. F. P. aloevorus Haran sp. nov., holotype ♂. Scale bars = 500 µm. Copulatory sclerite not to scale.
Fig. 4 in Description of five new species in the genus Phlyctinus Schoenherr (Coleoptera, Curculionidae): a first step in deciphering the P. callosus complex
Fig. 4 (opposite page). Habitus in natura, host plants and biotopes of Phlyctinus Schoenherr, 1826 species. A. P. callosus (Schoenherr, 1826). B. P. xerophilus Haran sp. nov. C–D. P. grootbosensis Haran sp. nov. and its host plant, Osteospermum moniliferum L. E–F. P. planithorax Haran sp. nov. and its host plant, Hymenolepis crithmifolia (L.) Greuter. G–H. Biotope and host plant (Arctotis angustifolia L.) of P. littoralis Haran sp. nov. I–J. P. aloevorus Haran sp. nov. on its host plant, Aloe arborescens Mill., with details of feeding damage on floral peduncle
Supplementary material (buffet data set): Egeler, G.-A., von Rickenbach, F., & Baur, P. (2020). Menüwahl in der Hochschulmensa: Design & Durchführung Feldexperiment (NOVANIMAL Kurzbericht). ZHAW. https://doi.org/10.21256/zhaw-1408
<p>During the fieldexperiment in the NOVANIMAL Project several informations about the offer of the buffet were collected. The report of the fieldexperiment see:</p> <p><a href="https://zenodo.org/deposit/4115429">Egeler, G.-A. & Baur, P. (2020). Menüwahl in der Hochschulmensa: Fleisch oder Vegi? Ergebnisse eines 12-wöchigen Feldexperiments (NOVANIMAL Working Paper No. 5). ZHAW. https://doi.org/10.21256/zhaw-1405</a></p>
dataset for paper Vanhaebost J, Faouzi M, Mangin P, Michaud K: New reference tables and user-friendly Internet application for predicted heart weights. Int J Legal Med 2014, 128(4):615-620.
<p>The heart weight is the most important parameter in the determination of cardiac hypertrophy. The obtained heart weight value should be compared against tables of normal weights by age, gender and body weight and height</p> <p>In the study by Vanhaebost<em> et al</em>. has been shown in the Swiss population that the heart weight increases along with the increase of the body weight, body height, BMI and body surface area (BSA). The mean heart weight is greater in men than in women at a similar body weight. The reference tables for predicted heart weights obtained from this study are presented as an user-friendly internet application (<a href="http://calc.chuv.ch/Heartweight">http://calc.chuv.ch/Heartweight</a>) enabling the comparison of heart weights observed at autopsy with the reference values.</p>
FIG. 1. — Areas VI-V-VI in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 1. — Areas VI-V-VI patterns of the pharynx shaped by the ridges and furrows: A-C, Perinereis latipalpa (Schmarda, 1861) n. comb. with a λ-shaped pattern; D-F, Perinereis nuntia (Savigny in Lamarck, 1818) with a χ-shaped pattern; G-I, Perinereis larentukana (Grube in Peters, 1881) n. comb. with a υ-shaped pattern; J-L, Perinereis shikueii Glasby & Hsieh, 2006 with a ɔc-shaped pattern; A, D, G, J, dorsal portion of oral ring; B, E, H, K, same with a slightly irregular line drawings on the shape formed by AVI-V-VI pattern; C, F, I, L, symmetrical line drawings of the AVI-V-VI patterns. Scale bars: 1 mm. J, K, after Glasby & Hsieh (2006).
FIG. 4 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 4. — Perinereis latipalpa (Schmarda, 1861) n. comb. lectotype (NMHW 769a): A-F, parapodia, anterior view (numbers refer the chaetiger); A, B, with bent dorsal cirri; E, black arrowheads, points used for measuring entire length of distal lobe of dorsal ligule; white, same but for proximal lobe; F, with incomplete dorsal cirri; black arrowheads, central glandular patch; white, proximal patch; G, H, approach of notopodial homogomph spinigers (chaet. 39 and 60, respectively) (arrows point thick, separated teeth); I, Heterogomph spiniger (chaet. 60); inset: proximal teeth; J, neuropodial heterogomph falciger, supracicular (chaet. 60); K, same, subacicular (chaet. 60); black arrowheads, points used for measuring length of blade of the proximal end (a); white, same but for distal end (b); L, same, subacicular (chaet. 119), black arrowheads, points used for measuring length of the serrated region; white, same but for entire length of blade. Scale bars: A-F, 0.5 mm; G-L, 15 µm.
FIG. 8 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 8. — Perinereis larentukana (Grube in Peters, 1881) n. comb., syntypes (ZMB 863): A-D, I-K, from best-preserved specimen; E-H, L, from complete specimen; A, anterior region, dorsal view; B, prostomium, dorsal view (arrow points nuchal organ); C, left jaw, dorsal (left) and ventral (right) views; D, same, zoom-in, ventral view (arrows point canals); E, maxillary ring of pharynx, frontal view; F, oral ring, frontal view; G, same, dorsal view (arrow points distal portion of λ-shaped pattern); H, same, ventral view; I, approach of notopodial homogomph spiniger (chaet. 10) (arrow points slender, evenly spaced teeth); J, neuropodial heterogomph falciger, supracicular (chaet. 10); M, same, subacicular (chaet.10); L, posterior region, dorsal view. Scale bars: A, 3 mm; B, H, L, 1 mm; C, E-G, 0.5 mm; D, 0.1 mm; I-L, 15 µm.
FIG. 9 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 9. — Perinereis larentukana (Grube in Peters, 1881) n. comb. best-preserved syntype (ZMB 863): A-F, parapodia, anterior view (numbers refer the chaetiger); F, with bent ventral cirri. Scale bars: 0.5 mm.
FIG. 7 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 7. — Perinereis latipalpa (Schmarda, 1861) n. comb.: A-E, topotype of Perinereis namibia Wilson & Glasby, 1993, n. syn. (ZMB 4109b): A, maxillary ring of pharynx, frontal view; B, oral ring of pharynx, dorsal view (arrow points distal portion of λ-shaped pattern); C, same, ventral view; D, parapodium 74, anterior view; E, approach to homogomph spinigers (chaet. 74), notopodial (left), neuropodial supracicular (right) (arrows point thickened, separated teeth). F-K, Perinereis vallata (Grube & Kröyer in Grube, 1858), non-type (ZMB 3666); F, approach to neuropodial supracicular homogomph spiniger (chaet. 76) (arrow points barely thickened, evenly spaced teeth); G, anterior region, dorsal view; H, maxillary ring, frontal view (arrows point merged paragnaths); I, oral ring, dorsal view (arrow points distal portion of χ-shaped pattern); J, pharynx, ventral view; K, same, lateral view. Scale bars: A, D, H, 0.5 mm; B, C, G, I-K, 1 mm; E, F, 15 µm.
FIG. 5 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 5. — Perinereis latipalpa (Schmarda, 1861) n. comb., holotype of Neanthes latipalpa Kinberg, 1865 n. syn. (SMNH 37900): A, anterior region, dorsal view; B, pharynx, dorsal view (arrow points proximal overlap of areas V and VI); C, oral ring of pharynx, lateral view; D, same, ventral view; E, posterior region, ventral view; F-I, parapodia, anterior view (numbers refer the chaetiger); J, approach of notopodial homogomph spinigers (chaet. 45) (arrows point thicker, separated teeth); K, neuropodial heterogomph falciger, subacicular (chaet. 45); L, permanent microscope slide, mounted 27th parapodia (SMNH 37900, housed at the NHMUK). Scale bars: A, 2 mm; B-E, 1 mm; F-H, 0.5 mm; I, 0.3 mm; J, K, 15 µm.
FIG. 3 in Redescription of two overlooked species of the Perinereis nuntia complex and morphological delimitation of P. nuntia (Savigny in Lamarck, 1818) from the Red Sea (Annelida, Nereididae)
FIG. 3. — Perinereis latipalpa (Schmarda, 1861) n. comb: A, recent (above) and older (below) labels of the jars containing paralectotype materials at the Natural History Museum, Vienna (NMHW 771); B, C, lectotype (NMHW 769a); D-I, Paralectotype (NMHW 771); B, anterior region, dorsal view; C, posterior region, dorsal view; D, pharynx, anterior view (arrow points distal portion of λ-shaped pattern); E, same, ventral view; F, same, dorsal view; inset: entire λ-shaped pattern (arrow points proximal overlap of areas V and VI); G, same, lateral view (arrow points narrow gap); H, left jaw, dorsal (left) and ventral (right) views; I, same, zoom-in, ventral view (arrow: canals). Scale bars: B, C, 3 mm; D-G, 2 mm; H, 1 mm; I, 0.5 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.