Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
6,783
datasets available to search
ShareScore release 0.9.0
Dataset results
6,783 results for “orientator”
Figs 124–149 in On the Lomechusini fauna of the East Palaearctic and Oriental regions, with a focus on the genera Orphnebius and Amaurodera (Coleoptera: Staphylinidae: Aleocharinae)
Figs 124–149: Amaurodera schuelkei from Assam (124–126), A. gilvicornis (127–128), A. bicarinata (129–132), A. latisulcata (133–135), A. brevipes (136–140), A. migritheca (141–146), A. frondium (147–148), and Zyrastilbus almorensis (149): median lobe of aedeagus in lateral and in ventral view (124–125, 127–134, 136–139, 141–144); spermatheca (126, 135, 140, 145–148); median portion of pronotum (149). Scale bars: 124–125, 127–134, 136–139, 141–144: 0.5 mm; 126, 135, 140, 145, 147–148: 0.2 mm; 146, 149: 0.1 mm.
Figs 31–42 in On the Lomechusini fauna of the East Palaearctic and Oriental regions, with a focus on the genera Orphnebius and Amaurodera (Coleoptera: Staphylinidae: Aleocharinae)
Figs 31–42: Orphnebius pertortus (31), O. migrus (32–33), O. reticulipennis (34–36), Zyrastilbus almorensis (37–38), Pheidologitonetes bursata (39–40), and Rabdotodrusilla vara (41–42): forebody (31–32, 34, 37, 39, 41); elytra and abdomen (33); abdomen (35, 38, 40, 42); antero-lateral portion of abdomen in dorso-lateral view (36). Scale bars: 37–38: 1.0 mm; 31–36, 39–42: 0.5 mm.
Figs 150–172 in On the Lomechusini fauna of the East Palaearctic and Oriental regions, with a focus on the genera Orphnebius and Amaurodera (Coleoptera: Staphylinidae: Aleocharinae)
Figs 150–172: Amaurodera frondium (150–151), A calicitheca (152–158), A. discoidea, paratype (159), A. longisetosa (160–163), A. bulbosa (paratypes of A. discoidea from Sabah) (164–165), Rabdotodrusilla vara (166–169), and Witteia tensa (170–172): median lobe of aedeagus in lateral and in ventral view (150–155, 160–162, 164–165, 168–169, 170–171); apical portion of median lobe in ventral view (156); spermatheca (157–159, 163, 172); male tergite VIII (166); male sternite VIII (167). Scale bars: 150–155, 157–165: 0.5 mm; 166–172: 0.2 mm; 156: 0.1 mm.
Figs 53–71 in On Zyras sensu strictu in the East Palaearctic and Oriental regions III, with a focus on the Southeast of Continental Asia and the Sunda Islands (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 53–71: Zyras elegantulus, lectotype (53–55), Z. facundus, lectotype (56–58), Z. bryanti (59–62), Z. matangensis, holotype (63–65), Z. granulipennis, holotype (66–69), and Z. latibasalis (70–71): median lobe of aedeagus in lateral and in ventral view (53–54, 56–57, 59–60, 63–64, 66–67, 70–71); paramere (55, 58); male tergite VIII (61, 65, 68); male sternite VIII (62, 69). Scale bars: 0.2 mm.
Figs 260–277 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 260–277: Zyras morulus (260–265), Z. variolatus (266–270), Z. montanus (271–275), and Z. preangeranus from Java (276–277): forebody (260); antenna (261); abdomen (262); median lobe of aedeagus in lateral and in ventral view (263–264, 266–267, 271–272, 276–277); paramere (265, 268, 273); male tergite VIII (269, 274); male sternite VIII (270, 275). Scale bars: 260–262: 1.0 mm; 263–277: 0.5 mm.
Figs 208–226 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 208–226: Zyras parvicollis (208–211), Z. ambulans (212–215), Z. nitens, holotype (216–221), and Z. gratellus (Malaysia) (222–226): median lobe of aedeagus in lateral and in ventral view (208–213, 216–217, 222–223); paramere (214, 218, 224); male tergite VIII (219, 225); male sternite VIII (220, 226); apical lobe of paramere (215); postero–median portion of male sternite VIII (221). Scale bars: 208–214, 216–220, 222–226: 0.5 mm; 215, 221: 0.1 mm.
Figs 227–244 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 227–244: Zyras parahirtus (227–228, 231–232), Z. matangensis (229–230, 233), Z. gratellus (Sulawesi) (234–238), and Z. densissimus (239–244): median lobe of aedeagus in lateral and in ventral view (227–230, 234–235, 239–241); paramere (231, 236, 242); male tergite VIII (232, 237, 243); male sternite VIII (233, 238, 244). Scale bars: 227–233, 237–238, 243–244: 0.5 mm; 234–236, 239–242: 0.2 mm.
Figs 191–207 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 191–207: Zyras proximus (191–197; 191–192: Thailand; 193–197: India), Z. novinversus (198–202), Z. brevilobatus (203–205), and Z. parvicollis (206–207): median lobe of aedeagus in lateral and in ventral view (191–194, 198–199, 203–204); paramere (195, 200, 205); male tergite VIII (196, 201, 206); male sternite VIII (197, 202, 207). Scale bars: 0.5 mm.
Figs 156–173 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 156–173: Zyras longilobatus (156–160), Z. latilobatus (161–165), Z. alternans (166–169), and Z. hirtus (170–173; 170–171: Sri Lanka; 172–173: South India): median lobe of aedeagus in lateral and in ventral view (156–157, 161–162, 166–167, 170–173); paramere (158, 163); male tergite VIII (159, 164, 168); male sternite VIII (160, 165, 169). Scale bars: 0.5 mm.
Figs 174–190 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 174–190: Zyras gardneri (174–177), Z. hirsutiventris (178–181), Z. luteipes (182–186), and Z. russiceps (187–190): median lobe of aedeagus in lateral and in ventral view (174–175, 178–179, 182–183, 187–188); male tergite VIII (176, 180, 185, 189); male sternite VIII (177, 181, 186, 190); paramere (184). Scale bars: 0.5 mm.
Figs 117–133 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 117–133: Zyras kraatzi (117–120), Z. exasperatus (121–124), Z. pindarae (125–131), and Z. perforatus (132–133): median lobe of aedeagus in lateral and in ventral view (117–118, 121–122, 125–128, 132–133); male tergite VIII (119, 123, 130); male sternite VIII (120, 124, 131); paramere (129). Scale bars: 0.5 mm.
Figs 134–155 in On Zyras sensu strictu in the East Palaearctic and Oriental regions, with a focus on the faunas of the Himalaya, India, Sri Lanka, Thailand, and Sulawesi (Coleoptera: Staphylinidae: Aleocharinae: Lomechusini)
Figs 134–155: Zyras perforatus (134–135), Z. pallipes (136–139), Z. nigroaeneus, holotype (140–141), Z. condignus (142–147), Z. morvani, holotype (148–149), and Z. truncatus (150–155): male tergite VIII (134, 138, 140, 146, 148, 152); male sternite VIII (135, 139, 141, 147, 149, 153); median lobe of aedeagus in lateral and in ventral view (136–137, 142–143, 150–151); paramere (144–145); female tergite VIII (154); female sternite VIII (155). Scale bars: 0.5 mm.
and) 33 () mm 4.4: lenght total (. nov. spec vulcanalis Metolinus.) Cuoco,) 32. (S): mm photo 3.5 (): 34 lenght () mm total 3.5 (:. nov lenght. spec total (lanceolatus) 1959,. P KRAATZ of Habitus (filum: 34 – 32 Xanthopius Figs in New data on the Oriental Xantholinini. 44. New species and new records from Nepal, Malaysia, Vietnam, Philippines, Sumatra, and Sabah (Coleoptera Staphylinidae)
and) 33 () mm 4.4: lenght total (. nov. spec vulcanalis Metolinus.) Cuoco,) 32. (S): mm photo 3.5 (): 34 lenght () mm total 3.5 (:. nov lenght. spec total (lanceolatus) 1959,. P KRAATZ of Habitus (filum: 34 – 32 Xanthopius Figs
Cell orientation characteristics of the natural combs of honey bee colonies
<p>The cell orientation characteristics of the natural combs of honey bees have received much research attention. Although natural combs have been shown to be composed of cells with three orientations—vertical, intermediate (oblique), and horizontal—the proportion of comb cells in these three orientations varies. Knowledge of the comb-building preferences of honey bees is essential for the installation of wax comb foundations, and clarification of the cell orientation characteristics of natural honey bee combs is important for beekeeping. The purpose of this study was to determine the cell orientation characteristics of natural combs of Eastern honey bees (<i>Apis cerana cerana</i>) and Western honey bees (<i>Apis mellifera ligustica</i>). Newly built combs were used to measure the orientation of hexagonal cells and calculate the proportion of cells in different orientations relative to the total number of cells. The number of eggs laid by queens in the cells of different orientations was also determined. The orientation of cells in the natural combs of Eastern and Western honey bees was determined based on the value of the minimum included angle between the pair of parallel cell walls and a vertical line connecting the top and bottom bars of the movable frame in the geometric plane of the comb: 0°≤θ≤10°, 10°<θ≤20°, and 20°<θ≤30° for vertical, intermediate, and horizontal orientations, respectively. Natural combs were composed of cells with at least one orientation (vertical or horizontal), two orientations (vertical + intermediate (oblique) or vertical + horizontal), or three orientations (vertical + intermediate + horizontal), and the proportions of combs with the three aforementioned configurations differed. Both Eastern honey bees and Western honey bees preferred building combs with cells in a vertical orientation. Queens showed no clear preference for laying eggs in cells of specific orientations. The results of this study provide new insight that could aid the production and cutting of wax comb foundations of Eastern and Western honey bees. Our study highlights the importance of installing wax comb foundations compatible with the comb-building preferences of bees.</p>
Pupil dilation during orienting of attention and conscious detection of visual targets in patients with left spatial neglect
<p>Right Brain-Damaged patients (RBD) with left spatial neglect (N+), are characterised by deficits in orienting and re-orienting attention to stimuli in the contralesional left side of space. In a recent ERPs study with visual stimuli (Lasaponara et al., 2018) we have pointed out that the pathological attentional bias of N+ is matched with exaggerated novelty reaction and contextual updating of targets in the right ipsilesional space and reduced novelty reaction and contextual updating of targets in the left contralesional space. To characterise further the attentional performance of N+, here we measured Pupil Dilation (PDil), which is a reliable marker of noradrenergic-locus coeruleus activity and response to unexpected events/rewards. Compared to Neutral and Valid targets, N+ patients displayed a pathological reduction of PDil in response to infrequent Invalid targets in the left side of space, while in Healthy Controls (HC) and RBD without neglect (N-) the same targets enhanced PDil with respect to Neutral and frequent Valid targets. Invalid targets in the right side of space enhanced PDil in all experimental groups. Interestingly, both N- and N+ showed a consistent number of target omissions both in the left and right side of space. With respect to seen targets, N- showed reduced PDil in response to unseen targets both in the left and right side of space. In contrast, N+ had reduced PDil in response to unseen targets in the left side of space though not in the right side, where seen and unseen targets evoked comparable levels of PDil. These results disclose, for the first time, the PDil correlates of spatial attention in left spatial neglect and suggest that the pathological attentional bias suffered by N+ might enhance the autonomic responses reflected in PDil to unseen ipsilesional stimuli. This enhancement can contribute to biasing contextual updating and predictive coding of stimuli in the ipsilesional space, thus worsening the pathological attentional bias of N+.</p>
Figs 24–28 in Three new genera of Oriental scuttle flies (Diptera: Phoridae)
Figs 24–28. Tendcornphora microgenitalis sp. nov. male: 24 – left face of hypopygium; 25 – right face of hypopygium; 26 – front leg; 27 – hind femur, tibia and first two tarsal segments; 28 – wing.
Figs 19–23 in Three new genera of Oriental scuttle flies (Diptera: Phoridae)
Figs 19–23. Tendcornphora microgenitalis sp. nov. male. 19 – head; 20 – postpedicels; 21 – tips of postpedicels; 22 – scutellum; 23 – abdominal tergites.
Figs 1–8 in Three new genera of Oriental scuttle flies (Diptera: Phoridae)
Figs 1–8. Hippaphora viklundi sp. nov. female. 1 – dorsal view; 2 – dorsal view of head; 3 – ventral view of head; 4 – postpedicel; 5 – eye; 6 – wing plus haltere (h); 7 – hairs of dorsal face of abdomen; 8 – hind femora.
Propulsion of nano- and microcones by a traveling ultrasound wave: dependence on orientation and aspect ratio of the particles
<p>Supplementary data for the following manuscript: Johannes Voß, Raphael Wittkowski, "Propulsion of nano- and microcones by a traveling ultrasound wave: dependence on orientation and aspect ratio of the particles"</p>
FIGURES 9–12 in First Oriental record of genus Neostroblia Heinrich (Hymenoptera, Ichneumonidae, Ctenopelmatinae) with description of one new species
FIGURES 9–12. Neostroblia melana Sheng & Watanabe, sp. nov. Paratype. Female 9 First tergite, dorsal view 10 First tergite, lateral view. 11 Second tergite, dorsal view 12 Apical portion of metasoma, lateral view.
ScienceDex guides
Understand access before you commit
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.