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PLATE III. Trigonidium Rambur, 1839. (A–H), Trigonidium humbertianum (Saussure, 1878): A, Male; B, Female; C, Eyesrounded protruding; D–E, Fifth joint of maxillary palpi large and triangular; F, Anterior tibiae with tympanum on both sides; G, Female ovipositor curved, compressed, acute at apex; H, Male sub-genital plate feebly notched at apex. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE III. Trigonidium Rambur, 1839. (A–H), Trigonidium humbertianum (Saussure, 1878): A, Male; B, Female; C, Eyesrounded protruding; D–E, Fifth joint of maxillary palpi large and triangular; F, Anterior tibiae with tympanum on both sides; G, Female ovipositor curved, compressed, acute at apex; H, Male sub-genital plate feebly notched at apex.

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PLATE IIB. Paratrigonidium Brunner, 1893. (A–E), Paratrigonidium nitidum Brunner, 1893: A, Male elytra membranous & harpvein only one; B, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; C, Lateral field of tegmina inmale blackish, presenting 3 parallel veins and the fourth incomplete; D, The hind femur with a feeble brownish band/stripe; E, The female ovipositor fulvous at base, darkened in the middle. Trigonidium Rambur, 1839. (F–I), Trigonidium humbertianum (Saussure, 1878): F, Anterior tibiae with tympanum on both sides; G, Fifth joint of maxillary palpi large and triangular; H, Female ovipositor curved, compressed, acute at apex; I, Male sub-genital plate feebly notched at apex. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IIB. Paratrigonidium Brunner, 1893. (A–E), Paratrigonidium nitidum Brunner, 1893: A, Male elytra membranous & harpvein only one; B, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; C, Lateral field of tegmina inmale blackish, presenting 3 parallel veins and the fourth incomplete; D, The hind femur with a feeble brownish band/stripe; E, The female ovipositor fulvous at base, darkened in the middle. Trigonidium Rambur, 1839. (F–I), Trigonidium humbertianum (Saussure, 1878): F, Anterior tibiae with tympanum on both sides; G, Fifth joint of maxillary palpi large and triangular; H, Female ovipositor curved, compressed, acute at apex; I, Male sub-genital plate feebly notched at apex.

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PLATE IIA. Paratrigonidium Brunner, 1893. (A–K), Paratrigonidium nitidum Brunner, 1893: A–B, Male and female black, shining;the male with membranous elytra, while female elytra corneous, convex with plain, longitudinal veins. Vertex flattened and sloping; C, Head wide and black; antenae yellow with first joint black; D, Pronotum black, pubescent; E, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; F, Tympanum external; G, Male elytra membranous; H, The hind femurwith a feeble brownish band/stripe; I, Legs yellowish; J, Lateral field of tegmina in male blackish, presenting 3 parallel veins andthe fourth incomplete; K, The female ovipositor fulvous at base, darkened in the middle, cerci long. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IIA. Paratrigonidium Brunner, 1893. (A–K), Paratrigonidium nitidum Brunner, 1893: A–B, Male and female black, shining;the male with membranous elytra, while female elytra corneous, convex with plain, longitudinal veins. Vertex flattened and sloping; C, Head wide and black; antenae yellow with first joint black; D, Pronotum black, pubescent; E, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; F, Tympanum external; G, Male elytra membranous; H, The hind femurwith a feeble brownish band/stripe; I, Legs yellowish; J, Lateral field of tegmina in male blackish, presenting 3 parallel veins andthe fourth incomplete; K, The female ovipositor fulvous at base, darkened in the middle, cerci long.

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PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre.

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PLATE IB. Natula Gorochov, 1987. (A–K), Natula matsuurai (Sugimoto, 2001): A, Head; B, Maxillary palpi; C, Second tarsal segment; D, Tympanum on fore tibia; E, Forewing lateral view showing longitudinal veins; F, Hind femur without stripe; G, Male Forewing mirror longer than wide; H, Female sub-genital plate triangular; I, Male sub-genital plate longer than wide, hind margin with a small projected median lobe; J, Hind tibial spines (3 pairs) on both sides; K, Ovipositor upcurved with a dorsal groove in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IB. Natula Gorochov, 1987. (A–K), Natula matsuurai (Sugimoto, 2001): A, Head; B, Maxillary palpi; C, Second tarsal segment; D, Tympanum on fore tibia; E, Forewing lateral view showing longitudinal veins; F, Hind femur without stripe; G, Male Forewing mirror longer than wide; H, Female sub-genital plate triangular; I, Male sub-genital plate longer than wide, hind margin with a small projected median lobe; J, Hind tibial spines (3 pairs) on both sides; K, Ovipositor upcurved with a dorsal groove

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PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular.

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FIG. 1. — Dioscorea comorensis R in A new edible yam (Dioscorea L.) species endemic to Mayotte, new data on D. comorensis R.Knuth and a key to the yams of the Comoro Archipelago

FIG. 1. — Dioscorea comorensis R.Knuth: A, female inflorescences with basal ovaries reflexed and enlarging; B, female inflorescence with more ovaries reflexed and enlarging; C, immature infructescence; D, part of male inflorescence showing the flowers in cymules; E, male inflorescences; F, male flowers. Photos Nicole Crestey (A, B, D, E) and Jean-Noël Labat (C, F).

opencc-by-4.0Dec 2007View details →
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Fig. 5 in Die Arten der afrotropischen Gattung Neoplerochila D R , 1982 (Insecta, Heteroptera, Tingidae, Tinginae)

Fig. 5: Neoplerochila paleatseasi DUARTE RODRIGUES, 1982. - Fig. 6: Neoplerochila uniformis DUARTE RODRIGUES, 1987 (Holotypus). - Fig. 7: Neoplerochila weenenana (DRAKE, 1953) (Holotypus). - Fig. 8: Neoplerochila youngai DUARTE RODRIGUES, 1987 (Holotypus).

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Fig. 1 in Die Arten der afrotropischen Gattung Neoplerochila D R , 1982 (Insecta, Heteroptera, Tingidae, Tinginae)

Fig. 1: Neoplerochila dispar DUARTE RODRIGUES, 1982. - Fig. 2: Neoplerochila inflata DUARTE RODRIGUES, 1982. - Fig. 3: Neoplerochila katbergana (DRAKE, 1953) (Paratypus). - Fig. 4: Neoplerochila millari spec. nov. (Holotypus).

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Text-fig. 2. a–e – Rhinolophus aff. lemanensis: a – PCMRCh65, left mxl with P4–M3, Petersbuch 2, ventral view; b – PCMRCh79 right mnd with C inf., Petersbuch 2, lingual view; c – PCMRCh66, right C sup., Petersbuch 2, lingual view; d – BSP 1976 XXII 5515, left mnd with m2–3, Petersbuch 2, occlusal view; e – BSP 1974 XIV 1139, left mnd with p4–m1; Erkertshofen 2, occlusal view; f, i, k–m – R. dehmi: f – BSP 1974 XIV 1118, right C sup., Erkertshofen 2, lingual view; i – BSP 1976 XXII 5507, left mnd with p4–m1, Petersbuch 2, occlusal view; k – PCMRCh32, right mxl with C sup., P4–M1, Petersbuch 2, ventral view; l – PCMRCh37, left mnd with m1–2, Petersbuch 2, occlusal view; m – PCMRCh89, right mnd with C inf., Petersbuch 2, lateral view; g–h – R. cf. delphinensis: g – BSP 1976 XXII 5522, right mxl with P4, Petersbuch 2, ventral view; h – BSP 1962 XIX 4153, left mnd with m1–3, Erkertshofen 1, occlusal view; j, n, o – R. grivensis: j – PCMRCh43, left C sup., Petersbuch 2, lingual view; n – BSP 1976 XXII 5543, left mxl, Petersbuch 2, ventral view; o – BSP 1976 XXII 5548, left mnd with m2–3, Petersbuch 2, occlusal view. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)

Text-fig. 2. a–e – Rhinolophus aff. lemanensis: a – PCMRCh65, left mxl with P4–M3, Petersbuch 2, ventral view; b – PCMRCh79 right mnd with C inf., Petersbuch 2, lingual view; c – PCMRCh66, right C sup., Petersbuch 2, lingual view; d – BSP 1976 XXII 5515, left mnd with m2–3, Petersbuch 2, occlusal view; e – BSP 1974 XIV 1139, left mnd with p4–m1; Erkertshofen 2, occlusal view; f, i, k–m – R. dehmi: f – BSP 1974 XIV 1118, right C sup., Erkertshofen 2, lingual view; i – BSP 1976 XXII 5507, left mnd with p4–m1, Petersbuch 2, occlusal view; k – PCMRCh32, right mxl with C sup., P4–M1, Petersbuch 2, ventral view; l – PCMRCh37, left mnd with m1–2, Petersbuch 2, occlusal view; m – PCMRCh89, right mnd with C inf., Petersbuch 2, lateral view; g–h – R. cf. delphinensis: g – BSP 1976 XXII 5522, right mxl with P4, Petersbuch 2, ventral view; h – BSP 1962 XIX 4153, left mnd with m1–3, Erkertshofen 1, occlusal view; j, n, o – R. grivensis: j – PCMRCh43, left C sup., Petersbuch 2, lingual view; n – BSP 1976 XXII 5543, left mxl, Petersbuch 2, ventral view; o – BSP 1976 XXII 5548, left mnd with m2–3, Petersbuch 2, occlusal view.

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Text-fig. 6. Allosorex stenodus FEJFAR, 1966 – lower molars, Ivanovce, fissure 6523. a–d: m1 dext. (Z 28203 – OF 652364; a – buccal view, b – lingual view, c – occlusal view, d – distal view), e–h, o: lost m1 sin. (OF 652367; e – distal view, f, o – occlusal view, g – lingual view, h – buccal view), i–j, v: m2 dext. (Z 28206 – OF 6523; i – buccal view, j – lingual view, v – occlusal view), k–l: m1 dext. (Z 28204 – OF 6523; k – occlusal view, l – lingual view), m–n: m1 dext. (Z 28205 – OF 6523; m – occlusal view, n – buccal view), p–r: m1 sin. (Z 28213 – OF 6523; p –lingual view, q – occlusal view, r – buccal view), s–u: m1 sin. (Z 28215 – OF 652366; s – buccal view, t – lingual view, u – buccal view), w–x: m3 sin. (Z 28213 – OF 6523; w – occlusal view, x – lingual view). in Allosorex Stenodus Fejfar, 1966 (Eulipotyphla, Soricidae): Re-Description Of Type Material And Re-Interpretation Of Its Fossil Record

Text-fig. 6. Allosorex stenodus FEJFAR, 1966 – lower molars, Ivanovce, fissure 6523. a–d: m1 dext. (Z 28203 – OF 652364; a – buccal view, b – lingual view, c – occlusal view, d – distal view), e–h, o: lost m1 sin. (OF 652367; e – distal view, f, o – occlusal view, g – lingual view, h – buccal view), i–j, v: m2 dext. (Z 28206 – OF 6523; i – buccal view, j – lingual view, v – occlusal view), k–l: m1 dext. (Z 28204 – OF 6523; k – occlusal view, l – lingual view), m–n: m1 dext. (Z 28205 – OF 6523; m – occlusal view, n – buccal view), p–r: m1 sin. (Z 28213 – OF 6523; p –lingual view, q – occlusal view, r – buccal view), s–u: m1 sin. (Z 28215 – OF 652366; s – buccal view, t – lingual view, u – buccal view), w–x: m3 sin. (Z 28213 – OF 6523; w – occlusal view, x – lingual view).

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Text-fig. 4. Allosorex stenodus FEJFAR, 1966 – upper and lower incisors, Ivanovce, fissure 6523. a–g: upper left incisor (Z 28193 – OF 652360; a, f – buccal view, b, g – lingual view, c – anterior view, d – dorsal view, e – ventral view), h–i: upper right incisor (Z 28192 – OF 6523; h – buccal view, i – lingual view), j–m: lower right incisor (Z 28197 – OF 652363; j, m – buccal view, k – lingual view, l – dorsal view), n–o: lower right incisor (Z 28196 – OF 652362; n – lingual view, o – crown cross-section), p–q: lower right incisor (Z 28195 – OF 652361; p – lingual view, l – crown cross-section), r: lower left incisor (Z 28199 – OF 6523; lingual view). in Allosorex Stenodus Fejfar, 1966 (Eulipotyphla, Soricidae): Re-Description Of Type Material And Re-Interpretation Of Its Fossil Record

Text-fig. 4. Allosorex stenodus FEJFAR, 1966 – upper and lower incisors, Ivanovce, fissure 6523. a–g: upper left incisor (Z 28193 – OF 652360; a, f – buccal view, b, g – lingual view, c – anterior view, d – dorsal view, e – ventral view), h–i: upper right incisor (Z 28192 – OF 6523; h – buccal view, i – lingual view), j–m: lower right incisor (Z 28197 – OF 652363; j, m – buccal view, k – lingual view, l – dorsal view), n–o: lower right incisor (Z 28196 – OF 652362; n – lingual view, o – crown cross-section), p–q: lower right incisor (Z 28195 – OF 652361; p – lingual view, l – crown cross-section), r: lower left incisor (Z 28199 – OF 6523; lingual view).

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Fig. 67. Left G1s, Rathbunaja species. A–D, R. ursus n in Revision of the spider crab genus Maja Lamarck, 1801 (Crustacea: Brachyura: Majoidea: Majidae), with descriptions of seven new genera and 17 new species from the Atlantic and Indo-West Pacific

Fig. 67. Left G1s, Rathbunaja species. A–D, R. ursus n. sp., holotype male (50.1 × 41.5 mm) (NMCR, ex ZRC 2013.1275), Philippines; E–G, R. brevipes n. sp., holotype male (24.0 × 18.4 mm) (MNHN-IU-2011-2408), Papua New Guinea. A, E = 5.0 mm; B-G = 1.0 mm; F, G = 0.5 mm.

opencc-by-4.0May 2015View details →
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Text-fig. 6. Fossil endocasts of large mammals from Gánovce-Hrádok Neanderthal site. a) Equidae gen. et sp. indet. (NM-Rv 21008); b) Equidae gen. et sp. indet. (NM-Rv 21007); c) Equidae gen. et sp. indet. (NM-Rv 21006); d) Bovidae gen. et sp. indet. (NM-Rv 21009); e) Ursus ex gr. spelaeus (NM R-604); f) Ursus ex gr. spelaeus (NM-Rv 21010); lateral and dorsal (except for f: ventral) views; lateral view for d and f are inverted. in Revised Floral And Faunal Assemblages From Late Pleistocene Deposits Of The Gánovce-Hrádok Neanderthal Site -Biostratigraphic And Palaeoecological Implications

Text-fig. 6. Fossil endocasts of large mammals from Gánovce-Hrádok Neanderthal site. a) Equidae gen. et sp. indet. (NM-Rv 21008); b) Equidae gen. et sp. indet. (NM-Rv 21007); c) Equidae gen. et sp. indet. (NM-Rv 21006); d) Bovidae gen. et sp. indet. (NM-Rv 21009); e) Ursus ex gr. spelaeus (NM R-604); f) Ursus ex gr. spelaeus (NM-Rv 21010); lateral and dorsal (except for f: ventral) views; lateral view for d and f are inverted.

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Figure 14. Antennae. A, Agalope trimacula. B, Rhodopsona rutila. C, D, Eterusia aedea formosana. E, Cyclosia midama. F, Heteropan scintillans. G, H, Callizygaena glacon. I, Adscita statices. J, Inouela formosensis. K, Zygaena filipendulae. L, Phauda mimica. M, N, Lactura dives. O, Anomoeotis levis. P, Himantopteus fuscinervis. Q, R in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)

Figure 14. Antennae. A, Agalope trimacula. B, Rhodopsona rutila. C, D, Eterusia aedea formosana. E, Cyclosia midama. F, Heteropan scintillans. G, H, Callizygaena glacon. I, Adscita statices. J, Inouela formosensis. K, Zygaena filipendulae. L, Phauda mimica. M, N, Lactura dives. O, Anomoeotis levis. P, Himantopteus fuscinervis. Q, R, Chalcosiopsis variata.

opencc-by-4.0Feb 2005View details →
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Figure 12. Placoid scales. A–D, morphotype 1. A–B, A, occlusal view. B, lateral view. C–D, C, occlusal view. D, lateral view. E–H, morphotype 2. E, occlusal view. F, lateral view. G, posterior view. H, anterior view. I–L, morphotype 3. I, occlusal view. J, lateral view. K, posterior. L, anterior. M–P, morphotype 4. M, occlusal view. N, lateral view. O, posterior view. P, anterior view. Q–U, morphotype 5. Q, occlusal view. R, lateral view. S, lateral view. T, posterior view. U, anterior view. V–Y, morphotype 6. V, anterior view. W, lateral view. X, occlusal view. Y, posterior view. All scale bars equal 0.5 in Neoselachians (Chondrichthyes, Elasmobranchii) from the Lower and lower Upper Cretaceous of north-eastern Spain

Figure 12. Placoid scales. A–D, morphotype 1. A–B, A, occlusal view. B, lateral view. C–D, C, occlusal view. D, lateral view. E–H, morphotype 2. E, occlusal view. F, lateral view. G, posterior view. H, anterior view. I–L, morphotype 3. I, occlusal view. J, lateral view. K, posterior. L, anterior. M–P, morphotype 4. M, occlusal view. N, lateral view. O, posterior view. P, anterior view. Q–U, morphotype 5. Q, occlusal view. R, lateral view. S, lateral view. T, posterior view. U, anterior view. V–Y, morphotype 6. V, anterior view. W, lateral view. X, occlusal view. Y, posterior view. All scale bars equal 0.5 mm.

opencc-by-4.0Feb 2009View details →
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Additional QCD Background Events for LHCO2020 R&D (signal region only)

<p>These are an additional ~610k QCD dijet background events, in the &quot;signal region&quot; region only (meaning, with mJJ in the range 3.3-3.7 TeV), produced using the same simulation settings as those of the <a href="https://doi.org/10.5281/zenodo.2629072">LHCO2020 R&amp;D Dataset</a>. The features are as described at that link:</p> <p>&#39;pxj1&#39;, &#39;pyj1&#39;, &#39;pzj1&#39;, &#39;mj1&#39;, &#39;tau1j1&#39;, &#39;tau2j1&#39;, &#39;tau3j1&#39;, &#39;pxj2&#39;, &#39;pyj2&#39;, &#39;pzj2&#39;, &#39;mj2&#39;, &#39;tau1j2&#39;, &#39;tau2j2&#39;, &#39;tau3j2&#39;</p> <p>They were used in <a href="https://arxiv.org/abs/2109.00546">CATHODE</a>&nbsp;for training the idealized anomaly detector and supervised classifier, as well as for final evaluation of all the anomaly detection methods.&nbsp;</p> <p><strong>Update September 22, 2023</strong></p> <p>An additional file was uploaded that contains&nbsp;the momentum 3-vectors of all the particles in each event, in addition to the 14 high level features listed above. As in the original LHCO R&amp;D dataset, up to 700 particles are included, with zero padding for events with fewer than 700 particles. So the shape of the dataset is&nbsp;</p> <pre>(612858, 2114)</pre> <p>with the first 2100 entries corresponding to the 3-momenta, in the order&nbsp;px0,py0,pz0,px1,py1,pz1,...,px699,py699,pz699;&nbsp;and the last 14 entries corresponding to the high level features listed above.&nbsp;</p>

opencc-by-4.0Dec 2021View details →
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Dataset with Curated Coronavirus-related R&D Outputs (1970 - March 2020)

<p><strong>The zip file includes metadata about R&amp;D outputs related to all </strong><a href="https://www.niaid.nih.gov/diseases-conditions/coronaviruses"><strong>Coronaviruses</strong></a>.</p> <p>The two main data sources used for this work include:</p> <ul> <li> <p><a href="https://docs.microsoft.com/en-us/academic-services/project-academic-knowledge/introduction"><strong>Microsoft Academic Graph (MSA) API</strong></a>: Subset of 10.000+ coronavirus R&amp;D outputs, with data from 1970, including patents and scientific publications.</p> </li> <li> <p><a href="https://www.grid.ac/"><strong>The Global Research Identifier Database (GRID)</strong></a><strong>:</strong> Used to enrich the organization data extracted from MSA.</p> </li> </ul> <p>After cleaning and enriching the data we extracted a total of <strong>1.100+ organization and</strong> <strong>26.700+ researchers</strong> spread across <strong>90+ countries</strong> and <strong>700+ cities</strong>.</p> <p>Inside the zip file&nbsp;you will find:&nbsp;</p> <ul> <li>documents.csv: Full list of documents</li> <li>topics.csv: list of topics connected to documents</li> <li>terms.csv: list of terms connected to documents</li> <li>people.csv: list of people (authors) connected to documents</li> <li>orgsplus.csv: list of organisations (incl their locations) connected to documents</li> </ul> <p>More information is available at&nbsp;<a href="https://app.gitbook.com/@dataverz/s/coronavirus-r-and-d/">https://app.gitbook.com/@dataverz/s/coronavirus-r-and-d/</a>&nbsp;</p>

opencc-by-4.0Apr 2020View details →
zenodo36/100

Figure 8. - Metasternal process (in the circle) and aedeagi of Dicronocephalusadamsidrumonti and Dicronocephalusadamsiadamsi. A, B, C, D Dicronocephalusadamsidrumonti (Tibet) E, F, G, H Dicronocephalusadamsidrumonti (Sichuan) I, J, K, L Dicronocephalusadamsiadamsi (South Korea) M, N, O, P Dicronocephalusadamsiadamsi (North Korea) Q, R, S, T Dicronocephalusadamsiadamsi (Dandong, China).

Figure 8. - Metasternal process (in the circle) and aedeagi of Dicronocephalusadamsidrumonti and Dicronocephalusadamsiadamsi. A, B, C, D Dicronocephalusadamsidrumonti (Tibet) E, F, G, H Dicronocephalusadamsidrumonti (Sichuan) I, J, K, L Dicronocephalusadamsiadamsi (South Korea) M, N, O, P Dicronocephalusadamsiadamsi (North Korea) Q, R, S, T Dicronocephalusadamsiadamsi (Dandong, China).

opencc-by-4.0Feb 2017View details →
zenodo36/100

Extended Signal Events for LHCO2020 R&D Dataset

<p>These are the extended signal events for the LHCO2020 R&amp;D dataset. It consists of the W'-&gt;X(qq)Y(qq) (2-prong decay) and the W'-&gt;X(qq)Y(qqq) (3-prong decay) events. The W' boson has a mass of 3.5 TeV, while the masses of particles X and Y form a grid ranging from 50 GeV to 600 GeV in 50 GeV increments. &nbsp;Each decay mode features 144 signal models, each with approximately 100,000 events. The events are produced using the same simulation settings as those of the <a href="https://doi.org/10.5281/zenodo.2629072">LHCO2020 R&amp;D Dataset</a>.</p> <p>The dataset includes high-level features of the two highest pT jets. They are the 3-momenta, pT, eta, phi, invariant masses, number of jet constituents, and n-subjettiness variables tau1, tau2, and tau3 for the highest pT jet (j1) and the second highest pT jet (j2) as well as the invariant masses of X and Y:</p> <pre>'pxj1', 'pyj1', 'pzj1', 'ptj1', 'etaj1', 'phij1', 'mj1', 'Nj1', 'tau1j1', 'tau2j1', 'tau3j1',<br>'pxj2', 'pyj2', 'pzj2', 'ptj2', 'etaj2', 'phij2', 'mj2', 'Nj2', 'tau1j2', 'tau2j2', 'tau3j2',<br>'mx', 'my'</pre> <p>Notice that the n-subjettiness variables use a different normalization scheme to the LHCO2020 R&amp;D Dataset, but the ratios of the variables should remain the same.</p>

opencc-by-4.0May 2024View details →

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record