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FIGURE 38. Chaetocnema hainanensis. A Male habitus. B Pronotum. C Head, frontal view. D Aedeagus, ventral view. E Aedeagus, lateral view. F in Revision of the Oriental Chaetocnema species (Coleoptera, Chrysomelidae, Galerucinae, Alticini)
FIGURE 38. Chaetocnema hainanensis. A Male habitus. B Pronotum. C Head, frontal view. D Aedeagus, ventral view. E Aedeagus, lateral view. F Apex of aedeagus, ventral view. G Vaginal palpi. H Spermatheca. I Pygidia (tergite 7) of females.
FIGURE 28. Chaetocnema duvivieri. A Male habitus. B Pronotum. C Head, frontal view. D Aedeagus, ventral view. E Aedeagus, lateral view. F in Revision of the Oriental Chaetocnema species (Coleoptera, Chrysomelidae, Galerucinae, Alticini)
FIGURE 28. Chaetocnema duvivieri. A Male habitus. B Pronotum. C Head, frontal view. D Aedeagus, ventral view. E Aedeagus, lateral view. F Apex of aedeagus, ventral view. G Vaginal palpi. H Spermatheca. I Tignum of female.
FIGURE 2. Stained lateral body scale removed from Sardinella alcyone n in Sardinella alcyone n. sp., a new sardine (Teleostei: Clupeiformes: Clupeidae) from the northwestern Pacific Ocean
FIGURE 2. Stained lateral body scale removed from Sardinella alcyone n. sp. (KAUM–I. 108335, paratype, 72.2 mm SL, Okinawa Island, Ryukyu Islands, Japan).
Fig. 3 Yphthimoides gabriela, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d in Uncovering the hidden diversity of the Neotropical butterfly genus Yphthimoides Forster (Nymphalidae: Satyrinae): description of three new species based on morphological and molecular data
Fig. 3 Yphthimoides gabriela, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d Edeagus (dorsal view). e Edeagus (lateral view)
Fig. 8 Yphthimoides iserhardi, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d in Uncovering the hidden diversity of the Neotropical butterfly genus Yphthimoides Forster (Nymphalidae: Satyrinae): description of three new species based on morphological and molecular data
Fig. 8 Yphthimoides iserhardi, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d Edeagus (dorsal view). e Edeagus (lateral view)
Fig. 6 Yphthimoides bella, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d in Uncovering the hidden diversity of the Neotropical butterfly genus Yphthimoides Forster (Nymphalidae: Satyrinae): description of three new species based on morphological and molecular data
Fig. 6 Yphthimoides bella, male genitalia. a Lateral view. b Dorsal view. c Ventral view. d Edeagus (dorsal view). e Edeagus (lateral view)
Figs. 57–60 Meiosimyza rorida, third instar. 57 The abdominal segments, lateral view. 58 in Immature stages of Meiosimyza Hendel 1925 and related genera (Diptera, Lauxaniidae)
Figs. 57–60 Meiosimyza rorida, third instar. 57 The abdominal segments, lateral view. 58 The anterior spiracle, lateral view, the spiracle was forced to surface probably during manipulation with specimen. 59 The abdominal segments, dorsal view. 60 Detail of the anal division showing small pad behind the ambulatory lobes and the posterior spiracles, note the two peg sensilla, ventral view. ACW Anterior creeping welt, A3– A6 third to sixth abdominal segment, LCW lateral creeping welt, LP lateral process of anal division, PS posterior spiracles, VP ventral pad. Arrowheads Tubercles of abdominal segments
Fig. 10 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 10 Diagram (a) and schematic representations (b, c) of shoot system in Pinguicula moranensis based on fig. 2c in Grob et al. (2007). Abbreviations as in Fig. 2 of the present article. b Our preferred interpretation. c Our understanding of the interpretation adopted by Grob et al. (2007)
Fig. 6 Pinguicula alpina, late flower development. a Stage with ring-shaped gynoecium primordium. b-e Flowers with calyx aestivation visible. f in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 6 Pinguicula alpina, late flower development. a Stage with ring-shaped gynoecium primordium. b-e Flowers with calyx aestivation visible. f Flower with lower lip sepals removed to show young spur of corolla. Abbreviations: g, gynoecium; pl, lower lip petals; pu, upper lip petals; s, spur, sl, lower lip sepals; su, upper lip sepals; st, stamen. Scale bars 0100 μm (a), 200 μm (b), 300 μm (e), 500 μm (c, d), 1,000 μm (f)
Fig. 1 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 1 Shoots of Pinguicula alpina with different chiralities. Frontal view of shoot apices (a, c) and their diagrams (b, d). In a and b (collected 1 September 2006), eight leaves (a-h) form an anticlockwise spiral. In c and d (collected 1 September 2006), ten leaves (a-j) form a clockwise spiral. 1, 2, 3 are flowers that are formed on a shoot of preceding order. Scale bars 0500 μm. In figs. 1, 2, 3, 4, leaves and flowers of the main axis are numbered starting from the first wellvisible leaf or flower. So, in fig. 1, a number of foliage leaves preceded flowers on the main axis
Fig. 4 Larinus hedenborgi pupa habitus. A Ventral view. B Lateral view. C in Morphological and molecular inference of immature stages of Larinus hedenborgi (Col: Curculionidae), a trehala-constructing weevil
Fig. 4 Larinus hedenborgi pupa habitus. A Ventral view. B Lateral view. C Dorsal view. Abbreviations: Ab1-9 number of abdominal segments, Th1-3 number of thoracic segments, ur urogomphi. Scale bar 10 mm
Fig. 2 Zenarge turneri larva. a Habitus, lateral view. b–d Head. b Posterior view. c Frontal view. d Lateral view. e in Comparative anatomy of the larvae of argid sawflies (Hymenoptera: Argidae): a phylogenetic approach
Fig. 2 Zenarge turneri larva. a Habitus, lateral view. b–d Head. b Posterior view. c Frontal view. d Lateral view. e Antenna. Abbreviations: anc, antacorium; ant, antenna; ata, anterior tentorial arms; atp, anterior tentorial pits; clp, clypeus; cls, clypeo-labral suture; crd, cardo; cs, coronal sulcus; ct, corporotentorium; e, eye; es, epistomal suture; fm, foramen magnum; fr, frons; ge, gena; lbp, labial palp; lm, labrum; lvp, larvapod; mxp, maxillary palp; md, mandible; n, notum; occ, occiput; ocu, ocularium; ocs, occipital sulcus; pf, palpifer; pgb, postgenal bridge; pgn, postgena; prm, prementum; psm, postmentum; sp, spiracle; st, stipes; v, vertex; vs, vertical sulcus
FIGURE 4. Randia sulbahiana. A. Branch with male inflorescence. B. Calyx. C. Branch with fruit. D. Fruit, lateral view. E. Fruit, frontal view. F. Fruit, with pilled seeds. A, B in Novelties in Randia L. (Gardenieae, Rubiaceae) from Brazil
FIGURE 4. Randia sulbahiana. A. Branch with male inflorescence. B. Calyx. C. Branch with fruit. D. Fruit, lateral view. E. Fruit, frontal view. F. Fruit, with pilled seeds. A, B. Amorim et al. 4469, C–F. Amorim et al. 6359. Photograph by A. M. Amorim.
Figure 4. Lateral hindfoot. A in Molecular phylogeny of Chinese raspy crickets (Orthoptera: Gryllacrididae) reveals incongruences in current classification
Figure 4. Lateral hindfoot. A, Apt. quadrimaculata; B, Apt. digitate; C, Apt. huanglianensis; D, Apt. biloba; E, T. huanglianensis sp. nov.; F, Ni. testaceus (arrow in F indicates extremely extended spine in the middle of hind tibia).
Figure 17. A–C. Chrysis mediadentata Linsenmaier, 1951, female from Scotland. A. Habitus, dorsal view. B. Habitus, lateral view. C in A journey through the history of the British Chrysididae (Hymenoptera): unexpected taxonomic problems, new records and description of a new species
Figure 17. A–C. Chrysis mediadentata Linsenmaier, 1951, female from Scotland. A. Habitus, dorsal view. B. Habitus, lateral view. C. Metasoma, dorso-lateral view, arrows pointing to: (i) punctation at base of second tergum, (ii) punctation at the apex of second tergum; (iii) position and shape of the median teeth on the apex of the third tergum. D. Chrysis solida Haupt, 1957, from England, metasoma, dorso-lateral view.
Figure 11. Cleptes mesosoma, A–E dorsal view, F lateral view. A in A journey through the history of the British Chrysididae (Hymenoptera): unexpected taxonomic problems, new records and description of a new species
Figure 11. Cleptes mesosoma, A–E dorsal view, F lateral view. A. Cleptes britannicorum sp. n., male, holotype. B. Cleptes semicyaneus, male, holotype. C. Cleptes nitidulus, male, from England. D. Cleptes britannicorum sp. n., male, holotype. E, F. Cleptes semicyaneus, male, holotype.
FIG. 10 in Organization and Ontogeny of a Complex Lateral Line System in a Goby (Elacatinus lori), with a Consideration of Function and Ecology
FIG. 10. Ontogeny of neuromast distribution in E. lori derived from fluorescent images. (A) 0 dph, 3 mm TL; (B) 10 dph, 4.5 mm SL; (C) 20 dph, 6.5 mm SL; (D) 31 dph, 9 mm SL; and (E) 38 dph, 9 mm SL presettlement larva. Pectoral fin removed to facilitate visualization of all neuromasts on the trunk. Yolk sac not drawn. Scale bar ¼ 1 mm. See Figures 3 and 4 for identity of neuromasts.
FIG. 2 in Organization and Ontogeny of a Complex Lateral Line System in a Goby (Elacatinus lori), with a Consideration of Function and Ecology
FIG. 2. Neuromast distributions in E. lori vitally stained with 4-di-2-ASP (lateral view, rostral to the left). (A) 0 dph (3 mm NL; yolk sac larva, fin folds still present) with only nine neuromasts present on head. By 1 dph, the yolk sac is fully absorbed and by 10 dph, flexion has started. (B) 38 dph (9.5 mm SL, pre-settlement) individual with all neuromast lines present on head; only the neuromasts in lines on operculum and mandible have begun to proliferate. Canal neuromasts are still visible (e.g., dorsal to orbit), indicating that the canals are not yet fully ossified. Settlement occurs at ~30–45 dph, 9–11 mm SL. (C) Wild-caught adult (42 mm SL) with lines of proliferated superficial neuromasts on head. (D) Trunk and tail of 20 dph (6 mm SL) larva. The few neuromasts on trunk will proliferate to become short vertical series of superficial neuromasts (see F). A few neuromasts on the caudal fin occur in three lines. (E) Anterior portion of the trunk (adult, 42 mm SL) illustrating several short lines of neuromasts. (F) Posterior portion of the trunk (adult, 42 mm SL) with well-organized vertical lines of neuromasts (''stitches'') on each myomere along horizontal septum. (G) Caudal fin (adult, 42 mm SL) with three lines (lines lc, lc1, and lc2) of densely placed neuromasts extending from the fin base to the tip of the caudal fin on the membranes between fin rays. Caudal-fin membranes are so thin that the neuromasts from both the left (white arrowhead) and right (yellow arrowhead) side are visible within a line. See Figures 3 and 4 for identification of neuromast lines.
FIG. 6 in Organization and Ontogeny of a Complex Lateral Line System in a Goby (Elacatinus lori), with a Consideration of Function and Ecology
FIG. 6. Neuromast and cupular morphology in E. lori. (A) Neuromast showing hair cells in central sensory strip with opposing polarities (hair cell orientation; double-headed arrow). (B) Detail of neuromast, as in A, showing ciliary bundles of individual hair cells (each with kinocilium [kc] and multiple stereocilia [sc]) with opposing polarities. (C) Gelatinous cupula (cu) retained on a neuromast that has the same orientation as neuromast in A; note the ''wing-like'' extensions of the cupula that reaches to the tips (arrows) of the elongate neuromast. (D) Neuromast that appears to be in the process of budding, which is thought to be the mechanism for neuromast proliferation. Double-headed arrows ¼ hair cell orientation.
FIG. 5 in Organization and Ontogeny of a Complex Lateral Line System in a Goby (Elacatinus lori), with a Consideration of Function and Ecology
FIG. 5. Lateral line development in E. lori. (A–E) Supraorbital (SO) canal with canal neuromasts (CNs) between orbits and superficial neuromasts in larvae. (A) CN (arrow) prior to canal enclosure (Stage I) at 0 dph. (B) CN (arrow) in depression as canal formation starts (Stage IIa) at 10 dph (5 mm SL). Nuclei of cells in two layers are visible in the neuromast (upper layer, sensory hair cells; lower layer, non-sensory support cells). (C) Left and right CNs (arrows) in the SO canal in the dorsal midline, with canal walls rising (*, Stage IIb), but not yet enclosing the CNs. (D) Left and right CNs (arrows, as in C; cupula of left neuromast is visible) are enclosed in the ossified SO canal (Stage IV; wild-caught settler, 14 mm SL). (E) Example of a line of densely placed superficial neuromasts (line c2) in wild-caught settler (14 mm SL) in the nasal area; prominent olfactory epithelium (oe). Stages of canal development (I–IV) follow Webb and Shirey (2003). (F–J) Ontogeny of superficial neuromast size and shape in E. lori showing diamond shape and gradual restriction of hair cells to a central, oval sensory strip. Axis of best physiological sensitivity (hair cell orientation) is perpendicular to the long axis of the neuromast. (F) 0 dph—neuromast on trunk is already diamond-shaped, (G) 10 dph—neuromast on trunk, (H) 20 dph—neuromast on cheek, (I) 34 dph—neuromast on cheek, note that sensory strip takes up a smaller portion of area of the neuromast compared to those in F–H. (J) Adult—superficial neuromast on caudal fin. Scale bars: A–E, 50 lm; F–H, 2 lm; I–J, 5 lm.
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.