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854 results for “Disparity”
FIGURE 5 in Morphological disparity despite genetic similarity; new species of Lobosorchis Miller & Cribb, 2005 (Digenea: Cryptogonimidae) from the Great Barrier Reef and the Maldives
FIGURE 5. Host distribution of species of Lobosorchis Miller & Cribb, 2005 mapped onto the phylogeny of Indo-West Pacific Lutjanidae produced by Miller and Cribb (2007a; b).
FIGURES 1–2. Hydryphantes clypeatus Thor, 1899 in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 1–2. Hydryphantes clypeatus Thor, 1899, larva: 1, dorsal view; 2, ventral view. Scale bar: 20 µm.
FIGURES 12–16. Hydryphantes clypeatus Thor, 1899 in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 12–16. Hydryphantes clypeatus Thor, 1899, female: 12, fragment of integument; 13, frontal plate; 14, capitulum; 15, chelicera; 16, pedipalp. Scale bars: 12, 16 = 50 µm, 14–15 = 100 µm, 13 = 200 µm.
FIGURES 27–31. H in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 27–31. H. dispar (Schaub, 1888), female: 27, fragment of integument; 28, frontal plate; 29, capitulum; 30, chelicera; 31, pedipalp. Scale bars: 27 = 50 µm, 31 = 100 µm, 28–30 = 200 µm.
FIGURES 19–26. H in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 19–26. H. dispar (Schaub, 1888), larva: 19–20, excretory pore plate; 21, chelicera, dorsal view; 22, pedipalp, ventrolateral view; 23, I-Leg-4–6; 24, II-Leg-4–6; 25, III-Leg-4–6; 26, claws of leg III. Simple setae on I–III-Leg-4–6 are not shown. Scale bars: 21 = 50 µm, 19-20, 23–26 = 20 µm.
FIGURES 34–41. H. planus Thon, 1899 in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 34–41. H. planus Thon, 1899, larva: 34–35, excretory pore plate; 36, chelicera, dorsal view; 37, pedipalp, ventrolateral view; 38, I-Leg-4–6; 39, II-Leg-4–6; 40, III-Leg-4–6; 41, claws of leg III. Simple setae on I–III-Leg-4–6 are not shown. Scale bars: 34–35, 37, 41 = 20 µm, 36, 38–40 = 50 µm.
FIGURES 42–45. H. planus Thon, 1899 in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 42–45. H. planus Thon, 1899, female: 42, frontal plate; 43, capitulum; 44, chelicera; 45, pedipalp. Scale bars: 42 = 200 µm, 43–44 = 100 µm, 45 = 50 µm.
FIGURES 17–18. H in Larval morphology of Hydryphantes clypeatus Thor, 1899, H. dispar Schaub, 1888 and H. planus Thon, 1899 (Acari, Hydrachnidia: Hydryphantidae)
FIGURES 17–18. H. dispar (Schaub, 1888), larva: 17, dorsal view; 18, ventral view. Scale bar: 20 µm.
FIGURE 2. Conchyliurus dispar n in Description of Conchyliurus dispar n. sp. (Copepoda, Cyclopoida, Clausidiidae) associated with the bivalve Barnea manilensis (Philippi) from the Yellow Sea with a discussion of the male morphotypes in the genus
FIGURE 2. Conchyliurus dispar n. sp., female. A, maxilla; B, maxilliped; C, leg 1; D, leg 2; E, third endopodal segment of leg 3; F, leg 4; G, free exopod segment of leg 5. Scale bars: A–B, 0.02 mm; C–G, 0.05 mm.
FIGURE 4. Conchyliurus dispar n in Description of Conchyliurus dispar n. sp. (Copepoda, Cyclopoida, Clausidiidae) associated with the bivalve Barnea manilensis (Philippi) from the Yellow Sea with a discussion of the male morphotypes in the genus
FIGURE 4. Conchyliurus dispar n. sp. (A, C) and Conchyliurus quintus Tanaka, 1961 (B, D–E). A, anal somite and caudal rami of female, ventral; B, anal somite and caudal rami of female, ventral; C, distal segment of female maxilla; D, distal segment of female maxilla; E, distal segment of male maxilla. Scale bars: A−B, 0.05 mm; C−E, 0.02 mm.
FIGURE 1. Conchyliurus dispar n in Description of Conchyliurus dispar n. sp. (Copepoda, Cyclopoida, Clausidiidae) associated with the bivalve Barnea manilensis (Philippi) from the Yellow Sea with a discussion of the male morphotypes in the genus
FIGURE 1. Conchyliurus dispar n. sp., female. A, habitus, dorsal; B, urosome, dorsal; C, antennule; D, antenna; E, labrum; F, mandible; G, paragnath; H, maxillule. Scale bars: A, 0.2 mm; B, 0.1 mm; C–D, 0.05 mm; E–F, H, 0.02 mm; G, 0.1 mm.
FIGURE 3. Conchyliurus dispar n in Description of Conchyliurus dispar n. sp. (Copepoda, Cyclopoida, Clausidiidae) associated with the bivalve Barnea manilensis (Philippi) from the Yellow Sea with a discussion of the male morphotypes in the genus
FIGURE 3. Conchyliurus dispar n. sp., male (A−F) and Conchyliurus quintus Tanaka, 1961, male (F). A, habitus of large male, dorsal; B, habitus of small male, dorsal; C, urosome of small male, ventral; D, spermatophore; E, maxilliped of large male; F, maxilliped of small male; G, urosome of small male, ventral. Scale bars: A−B, 0.2 mm; C, G, 0.1 mm; D−F, 0.05 mm.
FIGURES 12–13 in Spilogona dispar (Fallén, 1823) and its Palaearctic relatives (Diptera: Muscidae)
FIGURES 12–13. Armenia, Gegharkunik, the crater lake on Mt Armaghan, 2810 m, 15 July 2018, the type-locality of S. paradispar sp. nov..
FIGURES 4–7 in Spilogona dispar (Fallén, 1823) and its Palaearctic relatives (Diptera: Muscidae)
FIGURES 4–7. Abdominal markings of Spilogona: 4, S. paradispar sp. nov., male; 5, S. taeniata (Stein), male; 6, S. paradispar sp. nov., female; 7, S. taeniata (Stein), female. (4,6, Armenia, Aragatsotn, below Spitak Pass, 31.vii.2015, paratypes; 5, Armenia, Lake Kari, 21.vii.2015; 7, Georgia, Kazbegi, Sameba S, 2.vii.1983.)
FIGURES 8–11 in Spilogona dispar (Fallén, 1823) and its Palaearctic relatives (Diptera: Muscidae)
FIGURES 8–11. Male terminalia of Spilogona: 8, S. dispar (Fallén), hypopygium in lateral view; 9, S. dispar (Fallén), cercal plate in dorsal view; 10, S paradispar sp.nov., hypopygium in lateral view; 11, S. paradispar sp.nov., cercal plate in dorsal view. (8, 9, redrawn from Hennig (1959a, 1959b, as S. funeralis (Rondani); 10, 11, Armenia, Gegharkunik, the crater lake on Mt Armaghan, 15.vii.2018, paratypes.)
FIGURES 2–3 in Spilogona dispar (Fallén, 1823) and its Palaearctic relatives (Diptera: Muscidae)
FIGURES 2–3. Male head from in front: 2, Spilogona paradispar sp. nov.; and 3, Spilogona taeniata (Stein). (2, Armenia, Kotayk, Tsakhadzor, 30.vii.2015, paratype; 3, Armenia, Aragatsotn, Lake Kari, 21.vii.2015.)
Fig. 7 in Morphology-based phylogenetic analysis of South American Sericini chafers (Coleoptera, Scarabaeidae) contrasts patterns of morphological disparity and current classification
Fig. 7. Patterns of disparity derived from discrete morphological data: plots of axis 1 and 2 from principal coordinate analysis.
Fig. 6 in Morphology-based phylogenetic analysis of South American Sericini chafers (Coleoptera, Scarabaeidae) contrasts patterns of morphological disparity and current classification
Fig. 6. Single most parsimonious tree from implied weighting (K = 71.62) on the reduced data set (run 9), part 2. Support values (bootstrap/symmetric resampling) below 50 not shown.
Fig. 5 in Morphology-based phylogenetic analysis of South American Sericini chafers (Coleoptera, Scarabaeidae) contrasts patterns of morphological disparity and current classification
Fig. 5. Single most parsimonious tree from implied weighting (K = 71.62) on the reduced data set (run 9), part 1. Support values (bootstrap/symmetric resampling) below 50 not shown.
Fig. 4 in Morphology-based phylogenetic analysis of South American Sericini chafers (Coleoptera, Scarabaeidae) contrasts patterns of morphological disparity and current classification
Fig. 4. Characters illustrated: male genitalia. A-H) Aedeagus, dorsal view. A) Symmela beskei; B) S. varians; C) Astaena exquisita; D) A. leechi; E) A. longicornis; F) A. schnebli; G) A. sparsetosa; H) S. capixaba. Scale bars: A H) 0.5 mm.
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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.