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13,397 results for “sp. nov.”
Fig. 5 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 5. Topographical maps of photoreceptor nuclei of the nutria retina. In the three retinas analyzed, cell density was not equal for the different retinal areas, and there was no localization of the high-density region. (a) O-A3 right retina; (b) O-A4 right retina; (c) O-A5 left retina. Numbers in parentheses are the cell densities for the O-A5 map. N, nasal; V, ventral. Scale bar = 2 mm.
Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 4. Relative behavioral red sensitivity over the spawning cycle in female stickleback. Statistically significant differences (at p <0.05 Wilcoxon signed-rank test) between pairs of time-points are indicated by * (means ± SE; n = 7). The detail statistic results are given in the text.
Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 3. qPCR-determined expression ratios of (A) LWS-R:GPHN for eyeball and brain samples and (B) intron-free LWS-R to total LWS-R for eyeball samples from guppy and green swordtail. The box boundaries indicate the median (—), 25th and 75th percentiles (boxes), 95% range (|), and outliers (•).
Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 3. Mean behavioral red sensitivity of female stickleback in the spawning phase (0, 6, 72 and 96 h) and inter-spawning phase (24 and 48 h) (means ± SE; n = 7; p <0.028 Wilcoxon signed-rank test).
Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 2. Relative mRNA levels of retinal lws (A), rh2 (B), sws1 (C) and sws2 (D) (means ± SE; n = 6; *p <0.05 one-way Kruskal-Wallis test). Statistically significant differences in plasma testosterone and estradiol levels (at p <0.05 one-way Kruskal-Wallis test) are indicated by letters.
Fig. 1 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 1. Relative mRNA levels of retinal double cone opsins (lws and rh2) and single cone opsins (sws1 and sws2) in the spawning phase (0, 6 and 72 h after spawning; n = 18, note n refers to samples, each of which is pooled from two fish) and inter-spawning phase (24 and 48 h after spawning; n = 12) (means ± SE; *p <0.05 Mann-Whitney U test; the detail statistic results were shown in the text).
Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 6. Morphological comparison of fossil (red) and recent (black) dentition of Sparidae. A multivariate correspondence analysis (CA) with Chisquared distance was performed. The number of specimens used is indicated in parenthesis. Dataset is available in table S1.
Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 2. Pagrus major (Temminck and Schlegel, 1843), ASIZF0100141, from the Late Pleistocene Szekou Formation, Hengchun Peninsula, southern Taiwan. A, Lateral view of the nodule. B, Dorsal view of the anterior part of the nodule, note that fragments of the right jaws are exposed. C, Drawing of the recognized skull parts. See text for anatomical abbreviations. Scale bars = 10 mm.
Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 6. Macrobiotus naginae sp. nov. – egg chorion morphology and reproduction: A–B, egg surface under PCM; C, egg process under PCM; D, egg process under SEM; E, chorion surface between processes under PCM; F, chorion surface between processes under SEM; G, in toto egg under SEM; H, orcein-stained sperm inside male gonad under PCM; H, orcein-stained sperm inside female spermatheca under PCM. Flat arrowhead indicates the septum between process trunk and terminal disk: flat empty arrowhead indicates thickenings surrounding the processes; arrows indicate sperm nuclei. Scale bars: A–B, G–I = 10 μm; C–F = 2 μm.
Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 2. Macrobiotus naginae sp. nov. – habitus and cuticular pores: A, dorsoventral view of the body (Holotype; Hoyer's medium, PCM); B–C, cuticular pores on the dorsal part of the body under PCM (B) and under SEM (C). Flat arrowheads indicate pores on the dorsocaudal cuticle. Scale bars: A = 100 mm; B–C = 10 mm.
Fig. 1 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 1. Phylogenetic reconstruction of Macrobiotidae based on four concatenated markers (18S + 28S + COI + ITS2). Boxes delimit species of the Macrobiotus pseudohufelandi complex identified by ABGD performed on the COI alignment. Outgroups not shown. Values above branches represent node posterior probabilities (pp). pp = 1 not shown. All nodes with pp <0.70 were collapsed.
Fig. 1 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 1. Sampling site (A, B) and stratigraphic correlation (C) on the Hengchun Peninsula. (B) Szekou locality (black circle; modified from Chen 2016).
Fig. 5 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 5. Macrobiotus naginae sp. nov. – buccal apparatus and the oral cavity armature under PCM: A, dorsoventral view of the entire buccal apparatus; B–C, placoid morphology in ventral (B) and dorsal (C) view, respectively. D–G, oral cavity armature in dorsal (D–E) and ventral (F–G) view, respectively. Flat arrowhead indicates weak constrictions in the macroplacoids, flat empty arrowheads indicate third band of the Oral Cavity Armature (OCA), arrow indicates cuticular spikes between end of the buccal tube and anterior portion of the pharynx. Scale bars: A = 20 μm; B–G = 10 μm.
Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 4. Macrobiotus naginae sp. nov. – claws: A–B, claws I and IV, respectively, under PCM; C, claws IV under SEM. Flat arrowhead indicates an abnormal additional spur on the base on anterior claw IV; flat empty arrowheads indicate accessory points on primary branches. Scale bars = 10 μm.
Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 4. Osteological structures of Trichomycterus mutabilicolor Costa sp. nov. (a), mesethmoidal region and adjacent structures, middle and left portion, dorsal view; (b), left jaw suspensorium and opercular apparatus, lateral view; (c), middle and left portion of brachial arches, ventral view of dorsal elements on left, dorsal view of ventral elements on right; (d), left pelvic bone, ventral view. Abbreviations: ac4, accessory cartilage basibranchial 4; b2–3, basibranchials 2–3; bc4, cartilaginous basibranchial 4; c1–5, ceratobranchials 1–5; e1–4, epibranchials 1–4; h1–3, hypobranchials 1–3; p3, pharyngobranchial 3; lef, lateral ethmoid flap; pt4, pharyngobranchial 4 tooth-plate. Larger stippling represents cartilages.
Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 3. Habitat and live colouration of Trichomycterus mutabilicolor Costa sp. nov. (a), Cachoeira Mato Limpo, Riacho Pedacinho do Céu, upper Rio Paraitinga drainage, the type locality (23°09'25"S 44°5l'21"W); (b) Toca das Andorinhas, Rio Monjolo, upper Rio Paraitinga drainage (23°06'08"S 44°5l'56"W); (c) UFRJ 12649, 37.3 mm SL, paratype, DNA sequence used in the molecular analysis; (d) UFRJ 12650, 82.6 mm SL, holotype, DNA sequence used in the molecular analysis.
Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 4. Lysiosquilloides taiwanica sp. nov., male holotype, TL 145 mm (left raptorial claw missing), Hojie, Taiwan, NMMBA CD5609, colour in life. A, dorsal habitus; B, in habitat.
Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 3. Lysiosquilloides taiwanica sp. nov., male holotype, TL 145 mm, Hojie, Taiwan, NMMBA CD5609: A, anterior cephalothorax, dorsal view; B, rostral plate, dorsal view; C, ocular scales, dorsal view; D, ophthalmic somite ventral keel, right lateral view; E, right antennular peduncle, dorsal view; F, right antenna, lateral view; G, right raptorial claw, lateral view; H, right maxilliped 5 merus; I, right thoracic somites 6–8, dorsal view; J, thoracic somite 8 sternal keel, right lateral view; K–M, right pereopods 1–3, posterior view; N, posterior abdomen and right uropod, dorsal view; O, posterior telson, right lateral view; P, right uropod, ventral view; Q, right pleopod 1 endopod, anterior view. Scale: A, D–P = 5 mm; B, C, Q = 2.5 mm.
Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 4. Prevalence (value> 1.5) of all stages of R. filograna reproductive cells for different collection months. Mean temperatures and tendencies of temperature changes in the days before the collection of snails are shown at the top of the picture ↓ - decreasing tendency; ↑ - increasing tendency; ↕ - no clear tendency.
Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.
Fig. 3. Dynamics of appearance of mature reproductive cells in R. filograna. Data are means. See table 2 for values and SD for other stages of cells.
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.