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FIGURE 3. A–G in Description of fifty-one new species and new taxonomic arrangement for the E. sexdens group of the subgenus Edessa (Heteroptera, Pentatomidae, Edessinae, Edessa)

FIGURE 3. A–G. Edessa (E.) amaurata sp. n.: A–E, pygophore in dorsal, dorsolateral, ventral, posterior and posterolateral views, respectively; F, genital plates; G, metasternal process. vf 8—valvifer VIII; vf 9—valvifers IX; lat 8—laterotergite VIII; lat 9—laterotergite IX; X—tenth segment. Scale= 1 mm.

opennotspecifiedNov 2023View details →
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FIG. 22A. Cytology. A. Australiagraecia spina holotype. B. Australiagraecia spina, Cytol. prep. 81-81. C. Australiagraecia spina, South Australia Cytol. prep. 78-32. D. Australiagraecia helleri, Cytol. prep. 81-154. E. Australiagraecia helleri, Cytol. prep. 82-147. F. Australiagraecia minuta, Holotype. G. Australiagraecia tagera, Cytol. prep. 81-111 in Studies in Australian Tettigoniidae: New short-winged Agraeciini from Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)

FIG. 22A. Cytology. A. Australiagraecia spina holotype. B. Australiagraecia spina, Cytol. prep. 81-81. C. Australiagraecia spina, South Australia Cytol. prep. 78-32. D. Australiagraecia helleri, Cytol. prep. 81-154. E. Australiagraecia helleri, Cytol. prep. 82-147. F. Australiagraecia minuta, Holotype. G. Australiagraecia tagera, Cytol. prep. 81-111.

opennotspecifiedOct 2021View details →
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FIGURE. Illustration of Hedysarum sunhangii. a, plant; b, calyx; c, keel; d, standard; e, wings; f, mature article; g, seed; h, a single flower. Drawn from the holotype and isotype (a–h). in Hedysarum sunhangii (Fabaceae, Hedysareae), a new species from Pamir-Alay (Babatag Ridge - Uzbekistan)

FIGURE. Illustration of Hedysarum sunhangii. a, plant; b, calyx; c, keel; d, standard; e, wings; f, mature article; g, seed; h, a single flower. Drawn from the holotype and isotype (a–h).

opennotspecifiedOct 2021View details →
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Subspecies and Distribution. U. c. cinereoargenteus Schreber, 1775 — E USA. U. c. borealis Merriam, 1903 — SE Canada and USA (New England). U. c. californicus Mearns, 1897 — SW USA (S California). U. c. costaricensis Goodwin, 1938 — Costa Rica. U. c. flornidanus Rhoads, 1895 — Gulf of Mexico. U. c. fraterculus Elliot, 1896 — Mexico (Yucatan). U. c. furvus G. M. Allen & Barbour, 1923 — Panama. U. c. guatemalae G. S. Miller, 1899 — S Mexico S to Nicaragua. U. c. madrensis Burt & Hooper, 1941 — Mexico (S Sonora, SW Chihuahua & NW Durango). U. c¢. nigrirostris Lichtenstein, 1830 — SW Mexico. U. c. ocythous Bangs, 1899 — USA (Central Plains) and adjoining S Canada. U. ¢. orinomus Goldman, 1938 — S Mexico (Isthmus of Tehuantepec). U. c. perunsularis Huey, 1928 — NW Mexico (Baja California). U. c. scottit Mearns, 1891 — N Mexico and SW USA. U. c. townsend: Merriam, 1899 — W USA (California & Oregon). U. c. venezuelae]. A. Allen, 1911 — Colombia, Venezuela. in Canidae

Subspecies and Distribution. U. c. cinereoargenteus Schreber, 1775 — E USA. U. c. borealis Merriam, 1903 — SE Canada and USA (New England). U. c. californicus Mearns, 1897 — SW USA (S California). U. c. costaricensis Goodwin, 1938 — Costa Rica. U. c. flornidanus Rhoads, 1895 — Gulf of Mexico. U. c. fraterculus Elliot, 1896 — Mexico (Yucatan). U. c. furvus G. M. Allen & Barbour, 1923 — Panama. U. c. guatemalae G. S. Miller, 1899 — S Mexico S to Nicaragua. U. c. madrensis Burt & Hooper, 1941 — Mexico (S Sonora, SW Chihuahua & NW Durango). U. c¢. nigrirostris Lichtenstein, 1830 — SW Mexico. U. c. ocythous Bangs, 1899 — USA (Central Plains) and adjoining S Canada. U. ¢. orinomus Goldman, 1938 — S Mexico (Isthmus of Tehuantepec). U. c. perunsularis Huey, 1928 — NW Mexico (Baja California). U. c. scottit Mearns, 1891 — N Mexico and SW USA. U. c. townsend: Merriam, 1899 — W USA (California & Oregon). U. c. venezuelae]. A. Allen, 1911 — Colombia, Venezuela.

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S). in Atelidae

Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S).

opennotspecifiedMar 2013View details →
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FIGURE. Morphology of the studied Coelastrella strains. (1) SYKOA Ch-045-09. (2) SYKOA Ch-047-11. (3) SYKOA Ch-072-17. (А–D) vegetative cells and autosporangia. (E–G) cell wall ribs. (H) morphology of the old cells. Scale bar: 10μm. in Morphological and phylogenetic relations of members of the genus Coelastrella (Scenedesmaceae, Chlorophyta) from the Ural and Khentii Mountains (Russia, Mongolia)

FIGURE. Morphology of the studied Coelastrella strains. (1) SYKOA Ch-045-09. (2) SYKOA Ch-047-11. (3) SYKOA Ch-072-17. (А–D) vegetative cells and autosporangia. (E–G) cell wall ribs. (H) morphology of the old cells. Scale bar: 10μm.

opennotspecifiedNov 2021View details →
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FIGURE 11. Scanning electron micrographs. a, e, g, m in Revised classification of the New World Cylapini (Heteroptera: Miridae: Cylapinae): taxonomic review of the genera Cylapinus, Cylapoides and Peltidocylapus and a morphology-based phylogenetic analysis of tribe Cylapini

FIGURE 11. Scanning electron micrographs. a, e, g, m. Dorsal habitus; b, n. Lateral habitus; h, l. Scutellum; c, f, i. Thoracic pleura; d, j, o. Tarsus. k. Pretarsal claw. a–d. Cylapinus minusculus; e, f. Cylapoides unicolor; g–j. Peltidocylapus caudatus; k. Peltidocylapus calyciformis; l. Peltidocylapus ecuadorensis; m–o. Peltidocylapus scutellaris.

opennotspecifiedDec 2021View details →
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FIGURE. Phenological features of Ephedra aurea. A. San Vito lo Capo (locus classicus), natural habitat. B. Habit in natural places. C–D. Detail of ripe female cones. E. Twigs with male cones. F. Twigs with female cones. G. Internodes with scale-leaf. (Photos A, C, D, G by V. Ilardi, B, E, F by S. Cambria). in Ephedra aurea (Ephedraceae), a new species from Sicily

FIGURE. Phenological features of Ephedra aurea. A. San Vito lo Capo (locus classicus), natural habitat. B. Habit in natural places. C–D. Detail of ripe female cones. E. Twigs with male cones. F. Twigs with female cones. G. Internodes with scale-leaf. (Photos A, C, D, G by V. Ilardi, B, E, F by S. Cambria).

opennotspecifiedJan 2022View details →
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FIGURE. Puccinia magnusiana on Clematis sp. (A), Ranunculus chinensis (B–F) and Phragmites australis (G–K). A. Plants producing spermogonia and aecia on the hypertrophic stem. B. Vertical section of a spermogonium. C. Vertical section of an aecium surrounded with peridia. D. Aecia on the lower leaf surface. E. Acium observed under SEM. F. Aeciospores with verrucose surface observed under SEM. G. Aeciospores. H, I. Telia on the leaf surface. J. Teliospores. K. Vertical section of telia. Scale bars: B, K = 30 μm, C = 50 μm, E = 100 μm, F = 3 μm, G = 10 μm, J = 20 μm. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China

FIGURE. Puccinia magnusiana on Clematis sp. (A), Ranunculus chinensis (B–F) and Phragmites australis (G–K). A. Plants producing spermogonia and aecia on the hypertrophic stem. B. Vertical section of a spermogonium. C. Vertical section of an aecium surrounded with peridia. D. Aecia on the lower leaf surface. E. Acium observed under SEM. F. Aeciospores with verrucose surface observed under SEM. G. Aeciospores. H, I. Telia on the leaf surface. J. Teliospores. K. Vertical section of telia. Scale bars: B, K = 30 μm, C = 50 μm, E = 100 μm, F = 3 μm, G = 10 μm, J = 20 μm.

opennotspecifiedFeb 2022View details →
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FIGURE. Puccinia oncospora on Trillium kamtschaticum (A–D) and Phalaris arundinacea (E–G). A. Plants producing spermogonia and aecia on the leaf surface. B. Spermogonia and aecia on the lower leaf surface. C. Vertical section of a spermogonium. D. Aeciospores. E. Telia on the leaf surface. F. Teliospores. G. Vertical section of telia. Scale bars: C, D, F, G = 30 μm. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China

FIGURE. Puccinia oncospora on Trillium kamtschaticum (A–D) and Phalaris arundinacea (E–G). A. Plants producing spermogonia and aecia on the leaf surface. B. Spermogonia and aecia on the lower leaf surface. C. Vertical section of a spermogonium. D. Aeciospores. E. Telia on the leaf surface. F. Teliospores. G. Vertical section of telia. Scale bars: C, D, F, G = 30 μm.

opennotspecifiedFeb 2022View details →
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FIGURE. Puccinia caulophylli on Caulophyllum robustum (A–G) and Milium effusum (H–N). A. Plants producing spermogonia and aecia on leaf surface in the field. B. Vertical section of a spermogonium. C. Vertical section of an aecia surrounded with peridia. D, E. Aecia on the leaf surface observed by SEM. F. Aeciospores with verrucose surface observed by SEM. G. Aeciospores. H. Telia on the lower leaf surface. I. Uredinia on the leaf surface observed by SEM. J. Uredinia and telia on the leaf surface. K. Vertical section of an uredinium with paraphyses. L. Urediniospore observed by SEM. M. Vertical section of telia covered by host epidermis. N. Vertical section of a telium covered by host epidermis observed by SEM. Scale bars: B, G, N = 30 μm, C, E, I = 100 μm, F, L = 10 μm, K, M = 20 μm. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China

FIGURE. Puccinia caulophylli on Caulophyllum robustum (A–G) and Milium effusum (H–N). A. Plants producing spermogonia and aecia on leaf surface in the field. B. Vertical section of a spermogonium. C. Vertical section of an aecia surrounded with peridia. D, E. Aecia on the leaf surface observed by SEM. F. Aeciospores with verrucose surface observed by SEM. G. Aeciospores. H. Telia on the lower leaf surface. I. Uredinia on the leaf surface observed by SEM. J. Uredinia and telia on the leaf surface. K. Vertical section of an uredinium with paraphyses. L. Urediniospore observed by SEM. M. Vertical section of telia covered by host epidermis. N. Vertical section of a telium covered by host epidermis observed by SEM. Scale bars: B, G, N = 30 μm, C, E, I = 100 μm, F, L = 10 μm, K, M = 20 μm.

opennotspecifiedFeb 2022View details →
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FIGURE 1. Sinocrassula jiaozishanensis.—A. Habit.—B. Inflorescence.—C. Infructescence.—D, E. Leaf.—F, G. Bract.—H, I, J, K, L, M. Flowers.—N. Ovary.—O in Sinocrassula jiaozishanensis (Crassulaceae), a new species from Yunnan Province, China

FIGURE 1. Sinocrassula jiaozishanensis.—A. Habit.—B. Inflorescence.—C. Infructescence.—D, E. Leaf.—F, G. Bract.—H, I, J, K, L, M. Flowers.—N. Ovary.—O. Flower structure. Photographed by C. Chen.

opennotspecifiedMar 2022View details →
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Subspecies and Distribution. N.g.geoffroyiLeach,1821—WAustralia. N.g.pacificusJ.E.Gray,1831—E&SAustraliaandTasmaniaexceptNECoastofQueenslandandapparentlyincludesFraser,Kangaroo,King,andFlindersIs. N. g. pallescens Thomas, 1913 — N & C Australia. in Vespertilionidae

Subspecies and Distribution. N.g.geoffroyiLeach,1821—WAustralia. N.g.pacificusJ.E.Gray,1831—E&SAustraliaandTasmaniaexceptNECoastofQueenslandandapparentlyincludesFraser,Kangaroo,King,andFlindersIs. N. g. pallescens Thomas, 1913 — N & C Australia.

opennotspecifiedOct 2019View details →
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FIGURE. Brongniartia variabilis (Illustration by Óscar Dorado and Gerardo Cuevas). A. Branch with flowers, B. Foliole, C. Stipule, D. Flowers, E. Standard (front and lateral view), F. Wings petals, G. Keel petals, H. Calyx and androecium, I. Fruit, J. Indument of the stem. in Two new closely related species of Brongniartia (Fabaceae, Faboideae) from the Sierra Madre del Sur in Guerrero, México

FIGURE. Brongniartia variabilis (Illustration by Óscar Dorado and Gerardo Cuevas). A. Branch with flowers, B. Foliole, C. Stipule, D. Flowers, E. Standard (front and lateral view), F. Wings petals, G. Keel petals, H. Calyx and androecium, I. Fruit, J. Indument of the stem.

opennotspecifiedApr 2022View details →
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FIGURE. Brongniartia alvarezii (Illustration by Óscar Dorado and Gerardo Cuevas). A. Branch with fruits and flower, B. Foliole, C. Stipule, D. Flowers, E. Standard (front and lateral view), F. Wings petals, G. Keel petals, H. Calyx and androecium, I. Ovary, J. Fruit, K. Indument of the stem. in Two new closely related species of Brongniartia (Fabaceae, Faboideae) from the Sierra Madre del Sur in Guerrero, México

FIGURE. Brongniartia alvarezii (Illustration by Óscar Dorado and Gerardo Cuevas). A. Branch with fruits and flower, B. Foliole, C. Stipule, D. Flowers, E. Standard (front and lateral view), F. Wings petals, G. Keel petals, H. Calyx and androecium, I. Ovary, J. Fruit, K. Indument of the stem.

opennotspecifiedApr 2022View details →
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Subspecies and Distribution. S. g. grimmia Linnaeus, 1758 — S South Africa (Cape Province). S. g. altwallis Heller, 1912 — C Kenya (Aberdare Mts and Mt Kenya). S. g.caffra Fitzinger, 1869 — S Mozambique, E Zimbabwe, Swaziland, Lesotho, NE South Africa. S. g. campbelliae Gray, 1843 — E Guinea, S Mali, N Ivory Coast, S Burkina Faso, N Ghana, Togo, Benin, S Niger, Nigeria, N Cameroon, S Chad, Central African Republic, SW Sudan, W Uganda, Rwanda, Burundi. S. g. hindei Wroughton, 1910 — SE Kenya and N Tanzania. S. g. lobeliarum Lönnberg, 1919 — E Uganda, W Kenya (restricted to Mt Elgon). S. g. madoqua Ruppell, 1835 — W Ethiopia (highlands), W Eritrea. S. g nyansae Neumann, 1905 — SE Sudan, W Ethiopia, E Uganda, and W Kenya. S. g. orbicularis Peters, 1852 — S Somalia, E Kenya, Tanzania, E Zambia, Malawi, N Mozambique. S. g. splendidula Gray, 1871 — SE Gabon, S Republic of the Congo, S DR Congo, N Angola, E Botswana, W Zambia, W Zimbabwe. S. g. steinhardti Zukowsky, 1924 — S Angola, Namibia, W Botswana, NW South Africa. in Bovidae

Subspecies and Distribution. S. g. grimmia Linnaeus, 1758 — S South Africa (Cape Province). S. g. altwallis Heller, 1912 — C Kenya (Aberdare Mts and Mt Kenya). S. g.caffra Fitzinger, 1869 — S Mozambique, E Zimbabwe, Swaziland, Lesotho, NE South Africa. S. g. campbelliae Gray, 1843 — E Guinea, S Mali, N Ivory Coast, S Burkina Faso, N Ghana, Togo, Benin, S Niger, Nigeria, N Cameroon, S Chad, Central African Republic, SW Sudan, W Uganda, Rwanda, Burundi. S. g. hindei Wroughton, 1910 — SE Kenya and N Tanzania. S. g. lobeliarum Lönnberg, 1919 — E Uganda, W Kenya (restricted to Mt Elgon). S. g. madoqua Ruppell, 1835 — W Ethiopia (highlands), W Eritrea. S. g nyansae Neumann, 1905 — SE Sudan, W Ethiopia, E Uganda, and W Kenya. S. g. orbicularis Peters, 1852 — S Somalia, E Kenya, Tanzania, E Zambia, Malawi, N Mozambique. S. g. splendidula Gray, 1871 — SE Gabon, S Republic of the Congo, S DR Congo, N Angola, E Botswana, W Zambia, W Zimbabwe. S. g. steinhardti Zukowsky, 1924 — S Angola, Namibia, W Botswana, NW South Africa.

opennotspecifiedAug 2011View details →
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FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–j Araceae: a–b Anthurium angustifolium. c Anthurium longifolium. d Anthurium pentaphyllum. e Philodendron bernardopazii. f Philodendron hatschbachii. g Philodendron hederaceum. h Philodendron ornatum. i Philodendron pedatum. j Thaumatophyllum corcovadense. k Asplenium auriculatum (Aslpeniaceae). l Begonia solananthera. Bromeliaceae: m Aechmea araneosa. n Aechmea capixabae. o Aechmea castanea. in Augusto Ruschi Biological Reserve vascular epiphytes: a hotspot in the mountains of the Atlantic Forest of Southeastern Brazil

FIGURE. Vascular epiphytes representatives of the Augusto Ruschi Biological Reserve, Santa Teresa, Espírito Santo, Brazil. a–j Araceae: a–b Anthurium angustifolium. c Anthurium longifolium. d Anthurium pentaphyllum. e Philodendron bernardopazii. f Philodendron hatschbachii. g Philodendron hederaceum. h Philodendron ornatum. i Philodendron pedatum. j Thaumatophyllum corcovadense. k Asplenium auriculatum (Aslpeniaceae). l Begonia solananthera. Bromeliaceae: m Aechmea araneosa. n Aechmea capixabae. o Aechmea castanea.

opennotspecifiedMay 2022View details →
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Stu'g E'guh

The messianic tapeworm Source: Objaverse 1.0 / Sketchfab

opencc-byOct 2016View details →
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Figure 1 from: Leese F, Altermatt F, Bouchez A, Ekrem T, Hering D, Meissner K, Mergen P, Pawlowski J, Piggott J, Rimet F, Steinke D, Taberlet P, Weigand A, Abarenkov K, Beja P, Bervoets L, Björnsdóttir S, Boets P, Boggero A, Bones A, Borja Á, Bruce K, Bursić V, Carlsson J, Čiampor F, Čiamporová-Zatovičová Z, Coissac E, Costa F, Costache M, Creer S, Csabai Z, Deiner K, DelValls Á, Drakare S, Duarte S, Eleršek T, Fazi S, Fišer C, Flot J, Fonseca V, Fontaneto D, Grabowski M, Graf W, Guðbrandsson J, Hellström M, Hershkovitz Y, Hollingsworth P, Japoshvili B, Jones J, Kahlert M, Kalamujic Stroil B, Kasapidis P, Kelly M, Kelly-Quinn M, Keskin E, Kõljalg U, Ljubešić Z, Maček I, Mächler E, Mahon A, Marečková M, Mejdandzic M, Mircheva G, Montagna M, Moritz C, Mulk V, Naumoski A, Navodaru I, Padisák J, Pálsson S, Panksep K, Penev L, Petrusek A, Pfannkuchen M, Primmer C, Rinkevich B, Rotter A, Schmidt-Kloiber A, Segurado P, Speksnijder A, Stoev P, Strand M, Šulčius S, Sundberg P, Traugott M, Tsigenopoulos C, Turon X, Valentini A, van der Hoorn B, Várbíró G, Vasquez Hadjilyra M, Viguri J, Vitonytė I, Vogler A, Vrålstad T, Wägele W, Wenne R, Winding A, Woodward G, Zegura B, Zimmermann J (2016) DNAqua-Net: Developing new genetic tools for bioassessment and monitoring of aquatic ecosystems in Europe. Research Ideas and Outcomes 2: e11321. https://doi.org/10.3897/rio.2.e11321

Figure 1 - GANTT Diagram showing the planned COST Networking Tools to be applied to DNAqua-Net.

opencc-by-4.0Nov 2016View details →
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Figure 11. Nereis saramagoi. A, B, holotype. C, paratype 8. D, E, G, paratype 14. F, paratype 10. H, paratype 13. A in Revealing a new eyeless Nereis (Nereididae: Annelida) clade from deep-sea organic falls

Figure 11. Nereis saramagoi. A, B, holotype. C, paratype 8. D, E, G, paratype 14. F, paratype 10. H, paratype 13. A, anterior end, dorsal view. B, anterior end, ventral view. C, anterior end, dorsal view; arrow points to vestigial eyes covered by cuticle. D, pharynx dorsal view. E, pharynx, ventral view. F, anterior end, lateral view; arrow points to posterodorsal tentacular cirri. G, posterior end, pygidial cirri. H, anterior and median region of specimen. Scale bars: 0.5 mm in A, B; 1 mm in C–E, G; 2 mm in F; 5 mm in H.

opennotspecifiedSep 2023View details →

ScienceDex guides

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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