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FIGURE 6 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 6. Tridentella tanimbar sp. nov. Holotype. A, mandible; a, seta from molar process; B, maxillule; C, maxillule apex; D, maxilla; E, maxilla apex; F, maxilliped; G, maxilliped palp articles 4 and 5.
FIGURE 7 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 7. Tridentella tanimbar sp. nov. Holotype. A, pereopod 1; B, pereopod 1, merus inferior margin; C, pereopod 2;
FIGURE 8 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 8. Tridentella tanimbar sp. nov. Holotype. A–C, pleopods 1–3 respectively; D, uropod exopod, dorsal view; E, uropod exopod, ventral view; F, uropod endopod apex.
FIGURE 5 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 5. Tridentella tanimbar sp. nov. Holotype. A, dorsal view; B, lateral view; C, head; D, frons; E, pleotelson apex; F,
FIGURE 3 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 3. Tridentella memikat sp. nov. A, B, G, holotype, remainder paratype ♂ 33 mm. A, pereopod 1; B, pereopod 2; C, pereopod 1; D, pereopod 2; E, pereopod 3; F, pereopod 1 dactylus; G, pereopod 7.
FIGURE 4 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 4. Tridentella memikat sp. nov. Paratype ♂ except F, paratype & 27 mm. A–D, pleopods 1–3, 5; E, uropod exopod, ventral view; F, G, uropods dorsal view.
FIGURE 2 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 2. Tridentella memikat sp. nov. Paratype ♂ 33 mm. A, mandible; B, mandibular molar process; C, maxillule; D, maxillule apex; E, maxilla; F, maxilla apex; G, maxilliped; H, maxilliped endite, apex; I, maxilliped palp articles 4 and 5.
FIGURE 1 in New species of Tridentella Richardson, 1905 (Isopoda: Cymothoida: Tridentellidae), tropical marine isopod crustaceans from the Banda Sea, Indonesia
FIGURE 1. Tridentella memikat sp. nov. A–D, F, I, holotype; J, K, ♂ 33 mm and E, G and H, & 27 mm, paratypes. A, dorsal view; B, lateral view; C, head; D, frons; E, pleonites, lateral view; F, pleotelson, holotype; G, pleotelson, & paratype; H, pleotelson posterior margin, apex; I, penial processes, in situ; J, antennule; K, antenna peduncle.
FIGURE 10 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 10. Frontonia species from living cells (C, D, G, I, K, O, Q) and after silver nitrate impregnations (B, E, F, H, J, L, N, P). (A, B) F. azerbaijanica Alekperov, 2005 (after Alekperov 2005). (C) F. bullingtoni Dragesco, 1960 (after Dragesco 1960). (D) F. c a n e t i Dragesco, 1960 (after Dragesco 1960). (E, F) F. elongata Burkovsky, 1970 (after Burkovsky 1970b). (G, H) F. frigida Petz et al., 1995 (after Petz et al. 1995). (I, J) F. l y n n i Long et al. 2005 (after Long et al. 2005). (K, L) F. m a r i n a Fabre-Domergue, 1891 (K after Dragesco 1960; L after Roque 1961). (M, N) F. m a r i s a l b i Burkovsky, 1970 (after Burkovsky 1970a). (O, P) F. s a l m a s t r a Dragesco and Dragesco-Kernéis, 1986 (after Dragesco & Dragesco-Kernéis 1986). (Q) F. vacuolata Dragesco, 1960 (after Dragesco 1960). (R) F. vernalis Bullington, 1939 (after Bullington 1939). (S) F. canadensis Roque and Puytorac, 1972 (after Roque & Puytorac 1972). Scale bars in (C) = 25 µm; in (M) = 30µm; in(S) =50 µm; in (E) =60 µm; in (G) =90 µm; in (D,K, Q, R)= 100 µm; in (A)= 150 µm.
FIGURE 11 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 11. Small subunit rRNA gene sequence of Frontonia lynni (F. l y n n i) aligned with the sequence of F. d i d i e r i (F. didieri) and F. tchibisovae (F. t c h i b i s o.). Numbers at the end of lines indicate the number of nucleotides. The differences in sequence length were compensated for by introducing alignment gaps (-) in the sequences. Matched sites are marked with dots.
FIGURE 7 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 7. The Chinese population (except D and E) of Frontonia tchibisovae from living cells (A), after silver nitrate
FIGURE 9 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 9. The population of Frontonia tchibisovae in China after silver carbonate (A, E) and silver nitrate (B–D, F–J) impregnations. (A, F, G) Dorsal views, to show the CVP (arrowheads). (B, C) Buccal area, to show the oral apparatus, arrowheads in B mark the vestibular kineties. (D) Ventral view of a cell ingesting food. (E, J) Pellicle and silverline system structure. (H) Ventral view of a whole cell. (I) To show the paroral membrane (arrow) and the argentophilic line (arrowhead). Scale bars in (A) = 60 µm; in (H) = 80 µm.
FIGURE 8 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 8. The Chinese population of Frontonia tchibisovae from life (A–H). (A, B) Ventral views of two typical specimens. (C–E, G, H) To show the densely-arranged extrusomes (arrowheads). Arrows in C, G mark the buccal field. (F) Arrow indicates an ingested large alga in the cytoplasm. Scale bars in (A) = 65 µm; in (B) = 80 µm.
FIGURE 4. Frontonia multinucleata n in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 4. Frontonia multinucleata n. sp. from living cells (A, B), after silver nitrate (C, F, H, K), silver carbonate (I, J) and protargol (D, E, G) impregnations. (A, B) Ventral views of typical specimens. (C) Dorsal view, to show the contractile vacuole pore (arrowhead). (D, E) Side views, to show the fibers connected with the buccal and postoral suture area. Note the contractile vacuole is near the dorsal side. (F) Detailed structure of the peniculus 3. (G) To show the different situation of the macronuclear nodules. (H) The oral apparatus, note the two-rowed paroral membrane (PM) and the vestibular kineties (VK), in which the anterior part consists of monokinetids. (I, J) The infraciliature of ventral and dorsal (ventral-to-dorsal) side of the same specimen, to show the postoral suture (arrows in I and J), and the contractile vacuole. (K) Ventral view, note the long cytopyge (arrowheads). SL = silver line. Scale bars = 30 µm.
FIGURE 5. Frontonia multinucleata n in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 5. Frontonia multinucleata n. sp. from life (A–E). (A, D) Typical individuals. (B) To show the ejected extrusomes. (C) Extrusomes beneath the pellicle. (E) Lateral view, to show the contractile vacuole (arrow). Scale bars in (B) = 15 µm; in (D) = 45 µm; in (A, E) = 50 µm.
FIGURE 6. Frontonia multinucleata n in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 6. Frontonia multinucleata n. sp. after silver carbonate (A–C, E, F) and silver nitrate (D, G, H–N) impregnations. (A, B, E, F, M) Ventral and dorsal views of different cells. Note the macronuclear nodules (arrows). (C) Part of pellicle, arrow marks the extrusome. (D, H) Oral apparatus. Arrowheads mark the posterior ends of kinety rows in P3, which are in different lengths. (G, K) To point the CVP (arrowheads). (I) Detail of the silverline system. (J, L) Buccal area, to show the vestibular kineties (arrowheads) and the paroral membrane (arrow in L). (N) Structures posterior to the oral apparatus. Note the postoral kineties (arrowheads) and the cytopyge (arrow). Scale bars in (M) = 30 µm; in (A, E, F) = 45 µm; in (K) = 50 µm.
FIGURE 3. Frontonia didieri n in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 3. Frontonia didieri n. sp. from living cells (A, B, E, I, J), after silver carbonate (G, H), silver nitrate (C, D, K) and protargol (F) impregnations. (A) Ventral view, to show the typical body shape. (B, G) Anterior ventral part. Note the buccal cavity (arrow) and the extrusomes (arrowheads) in B. (C) Ventral view of a specimen. (D) To show the silverline system, arrow marks the CVP. (E) A pressed cell filled with diatoms. (F) Oral apparatus. Arrows indicate the vestibular kineties, arrowheads mark the posterior ends of kinety rows in P1, while double-arrowheads refer to the paroral membrane. (H) The macronucleus. (I) Arrow marks the CVP. (J) To show the contractile vacuole and the collecting canals (arrowheads). (K) To show the detail of the structure of P3. Note the shortest (arrowhead), the median-long (doublearrowheads) and the longest rows (arrow). Scale bars in (C) = 30 µm; in (J) = 40 µm; in (E) = 50 µm; in (A) = 70 µm.
FIGURE 2 in Taxonomic studies on three marine species of Frontonia from northern China: F. didieri n. sp., F. multinucleata n. sp. and F. tchibisovae Burkovsky, 1970 (Ciliophora: Peniculida)
FIGURE 2. Dorsal-lateral views of Frontonia didieri n. sp. (A–D) and F. t c h i b i s o v a e (E–H) (after silver nitrate impregnation), to show the CVP (arrowheads).
FIGURE 5 in Euphilomedes chupacabra (Ostracoda: Myodocopida: Philomedidae), a new demersal marine species from coastal Puerto Rico with male-biased vespertine swimming activity
FIGURE 5. Swimming activity of male Euphilomedes chupacabra. We collected males by dragging an aquarium net through the water adjacent to a lighted pier at approximately 15 minute intervals, averaging over two net passes for each data point (see methods for further details). We fit a Gaussian distribution to the data points to estimate two parameters, maximum density (number of males) and peak activity time (minutes after sunset), for each night we collected A. Data from July 15 and fitted Gaussian model are illustrated as a representative night of collecting. Here, peak activity was estimated to be at 106 minutes after sunset and maximum density was 177 males. B. Estimates of peak activity are plotted for each night of collecting. Shaded gray area represents moon illumination phase. C. Estimates of maximum density are plotted for each night of collecting. Shaded gray area represents moon illumination phase.
FIGURE 4 in Euphilomedes chupacabra (Ostracoda: Myodocopida: Philomedidae), a new demersal marine species from coastal Puerto Rico with male-biased vespertine swimming activity
FIGURE 4. Euphilomedes chupacabra, new species, adult male paratype SBMNH # 83216; A, carapace, right, inner view; B, first antenna, left, m. v., C, second antenna, left endopod, l.v., D, copulatory limb, right, l.v. All scale bars = 0.1 mm except for that in A, which = 1 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.