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.
13,017
datasets available to search
ShareScore release 0.9.0
Dataset results
13,017 results for “Positionning”
FIGURE 41 in Systematic position of Apodemia paucipuncta (Riodinidae), and a critical evaluation of the nymphidiine transtilla
FIGURE 41. Valva: dorsal processes closely adjacent to each other, fused or nearly so (0); separated (1). RC:0.464. Fig. 18 and 20. 42. Valva, when dorsal processes separated: dorsal processes extended to form a sclerotized bridge (i.e., dorsal bridge) (0), not extended to form a sclerotized bridge (1). RC:0.4. Fig. 6. The dorsal bridge described in 42:0 is likely not homologous to the ventral bridge described in character 48 (see Discussion).
FIGURES 9–17 in Systematic position of Ascopus Marshall, Oreosecus Marshall, Perarogula Hoffmann and Rhadinocopes Hustache (Coleoptera: Curculionidae: Entiminae) with description of a new species of Ascopus from Guinea
FIGURES 9–17. Structural details of Ascopus girardi sp. nov. 9. head with rostrum, dorsal view; 10. head with rostrum, lateral view; 11. femur and tibia of right foreleg; 12. penis, dorsal view; 13. tegmen, dorsal view; 14. sternite IX of male; 15. spermatheca; 16. sternite VIII of female, dorsal view; 17. ovipositor, dorsal view. Scale = 0.50 mm, only 17 = 0.25 mm.
FIGURES 1–4. Dorsal habitus. 1 in Systematic position of Ascopus Marshall, Oreosecus Marshall, Perarogula Hoffmann and Rhadinocopes Hustache (Coleoptera: Curculionidae: Entiminae) with description of a new species of Ascopus from Guinea
FIGURES 1–4. Dorsal habitus. 1. Ascopus lamottei (Hoffmann); 2. A. curvipes (Hustache); 3. A. echinatus (Marshall); 4. A. pyriformis Marshall. Scale = 1.00 mm.
FIGURES 5–8. Dorsal habitus. 5. A in Systematic position of Ascopus Marshall, Oreosecus Marshall, Perarogula Hoffmann and Rhadinocopes Hustache (Coleoptera: Curculionidae: Entiminae) with description of a new species of Ascopus from Guinea
FIGURES 5–8. Dorsal habitus. 5. A. girardi sp. nov.; 6. Tapinomorphus alticola (Hustache); 7. T. orientalis (Hustache); 8. T. porculus (Marshall). Scale = 1.00 mm.
FIGURE 36 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 36. Superficial bones of upper pectoral girdle showing course of lateral line in: A) Datnioides microlepis, ACG CS632, 30 mm SL; B) Equulites elongatus (Leiognathidae), AMS I.20829-018, 74 mm SL; C) Gazza minuta (Leiognathidae), AMS I.21841-016, 105 mm SL; D) Antigonia rhomboidea, AMS I.15526-006, 45 mm SL; E) Capros aper, BMNH 2016.4.47.169- 172, 51 mm SL. Laterosensory canals are shown in pink or red (where canals pass through supracleithrum in A–C); ventral arm of posttemporal truncated in A,B and D. Abbreviations: EX, extrascapula; PT, posttemporal; SCL, supracleithrum; TLL, trunk lateral line. Scale bars = 2 mm. Illustrations by A.C. Gill.
FIGURE 35 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 35. Anterior portion of dorsal fin and associated axial skeleton of A) Datnioides microlepis ACG CS632, 35 mm SL; B) Heniochus diphruetes (Chaetodontidae), ACG CS476, 47 mm SL; C) Equulites elongatus (Leiognathidae), AMS I.20829- 018, 74 mm SL; D) Capros aper, USNM 320065, 60 mm SL (pectoral girdle removed); E) Acanthurus olivaceus (Acanthuridae), ACG CS130, 39 mm SL. Abbreviations: DPT1, first dorsal pterygiophore; R1, first rib; SN, supraneurals; SOC, supraoccipital. White arrows indicate first neural spine; black arrows indicate vacant interneural spaces; scale bars = 5 mm. Photos by A.C. Gill.
FIGURE 31 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 31. Caudal skeleton of Hapalogenys darwiniensis, paratype, CSIRO H.4069-12, 75.5 mm SL. Methods of presentation follow Figure 29. Illustration by A.C. Gill.
FIGURE 46 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 46. Larva of Leiognathus equulus, 7.2 mm SL, AMS I.43616-037, from Taiwan (reared), after Soars & Leis (2010: fig. 1b). Scale bar is 1 mm. Illustration by J.M. Leis, N. Soars and S.B. Leis.
FIGURE 26 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 26. Dorsal gill arches of A) Antigonia rhomboidea, AMS I.15526-006, 45 mm SL; B) Capros aper, USNM 320065, 60 mm SL; C) Platax orbicularis (Ephippidae), ACG CS497, 27 mm SL; D) Scatophagus argus (Scatophagidae), ACG CS7, 40 mm SL. Gill rakers not shown. Abbreviations and methods of presentation follow Figures 20 and 24. Illustrations by A.C. Gill.
FIGURE 29 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 29. Caudal skeleton of Lobotes surinamensis, ASU 19554, 52 mm SL. Arrows indicate dorsalmost and ventralmost principal caudal-fin rays; cartilage shown in dark grey. Abbreviations: DPUC, dorsal preural cartilage; EP1-3, epurals 1-3; H1, hypural 1; H5, hypural 5; HS, haemal spine; NS, neural spine; PCS, proccurent spur; PH, parhypural; PU2, preural centrum 2; PU4, preural centrum 4; VPUC, ventral preural cartilage; UN1-2, uroneurals 1-2. Illustration by L. Hindes.
FIGURE 30 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 30. Caudal skeleton of Datnioides microlepis, ASU 19552, 43 mm SL. Methods of presentation follow Figure 29. Illustration by L. Hindes.
FIGURE 25 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 25. Dorsal gill arches of A) Heniochus diphruetes (Chaetodontidae), ACG CS476, 47 mm SL; B) Pomacanthus xanthometopon (Pomacanthidae), ACG CS285, 55 mm SL; C) Drepane punctata (Drepaneidae), NTM S.12373-002, 40 mm SL; D) Photolateralis moretoniensis (Leiognathidae), ACG CS 162, 58 mm SL. Gill rakers not shown. Abbreviations and methods of presentation follow Figures 20 and 24. Illustrations by A.C. Gill.
FIGURE 48 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 48. Larva of an unidentified species of Antigonia, 5.9 mm SL, AMS I.31952-001, from the Australian NW Shelf, after Leis & Trnski (2000: fig. 35E). Illustration by J.M. Leis and T. Trnski. Note scales shown only on cheek, in profile ventrally on trunk and in a representative patch above pectoral fin; supraoccipital-spine tip broken.
FIGURE 22 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 22. Right-side pharyngobranchial toothplates in ventral view of representative acanthuriform fishes: A) Hapalogenys darwiniensis, paratype, CSIRO H.4069-12, 75.5 mm SL; B) Lobotes surinamensis, ASU 19554, 52 mm SL; C) Datnioides micolepis, ASU 19552, 43 mm SL; D) Heniochus diphruetes (Chaetodontidae), ACG CS476, 47 mm SL; E) Pomacanthus xanthometopon (Pomacanthidae), ACG CS285, 55 mm SL; F) Drepane punctata (Drepaneidae), NTM S.12373-002, 40 mm SL; G) Photolateralis moretoniensis (Leiognathidae), ACG CS 162, 58 mm SL; H) Antigonia rhomboidea, AMS I.15526-006, 45 mm SL (left side, reversed); I) Capros aper, USNM 320065, 60 mm SL; J) Platax orbicularis (Ephippidae), ACG CS497, 27 mm SL; K) Scatophagus argus (Scatophagidae), ACG CS7, 40 mm SL; L) Siganus spinus (Siganidae), ACG CS572, 61 mm SL; M) Zanclus cornutus (Zanclidae), ACG CS601, 66 mm SL; N) Naso brevirostris (Acanthuridae), ACG CS858, 51 mm SL. Abbreviations: PB2-3 TP, pharygnobranchial 2-3 tooth plates; PB4TP, pharyngobranchial 4 toothplate. Tooth plate orientations refer to in situ positions; anterior to top. Scale bars = 0.2 mm (C, D, F, H, J) or 0.5 mm (A, B, E, G, I, K, L, M, N). Illustrations by A.C. Gill.
FIGURE 28 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 28. Outline drawings in lateral view of interopercle (IOP), retroarticular (RA), anguloarticular (AA), dentary (DEN) and interoperculo-mandibular ligament (IML) of: A) Datnioides micolepis, ASU 19552, 43 mm SL; B) Lobotes surinamensis, ASU 19554, 52 mm SL; C) Hapalogenys darwiniensis, paratype, CSIRO H.4069-12, 75.5 mm SL; D) Heniochus diphruetes (Chaetodontidae), ACG CS476, 47 mm SL; E) Pomacanthus xanthometopon (Pomacanthidae), ACG CS285, 55 mm SL; F) Drepane punctata (Drepaneidae), NTM S.12373-002, 40 mm SL; G) Equulites elongatus (Leiognathidae), AMS I.20829-018, 74 mm SL; H) Antigonia rhomboidea, AMS I.15526-006, 45 mm SL; I) Capros aper BMNH 2016.4.47.169-172, 51 mm SL; J) Platax orbicularis (Ephippidae), ACG CS497, 27 mm SL; K) Scatophagus argus (Scatophagidae), ACG CS7, 40 mm SL; L) Siganus spinus (Siganidae), ACG CS572, 61 mm SL; M) Luvarus imperialis (Luvaridae), USNM 228612, 79.2 mm SL (redrawn from Tyler et al. 1989: fig. 44); N) Zanclus cornutus (Zanclidae), ACG CS601, 66 mm SL; O) Naso brevirostris (Acanthuridae), ACG CS858, 51 mm SL. Dotted lines indicate portion of anguloarticular obscured by dentary. Scale bars = 2 mm (A, B, D, E, F, G, H, I, J, K, O) or 5 mm (C, M, N). Illustrations by A.C. Gill.
FIGURE 23 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 23. Anterior part of skull of: A) Hapalogenys dampieriensis, CSIRO H 4069-12 (paratype), 75.5 mm SL (right side, reversed); B) Drepane punctata (Drepaneidae), NTM S.12373-002, 40 mm SL (right side reversed); C) Antigonia rhomboidea, AMS I.15526-006, 45 mm SL; D) Capros aper, BMNH 2016.4.27.169-172, 51 mm SL. Cartilage shown in dark grey. Abbreviations: ETH, ethmoid; ETHC, ethmoid cartilage; FR, frontal; LETH, lateral ethmoid; PSPH, parasphenoid; VOM, vomer. Illustrations by A.C. Gill.
FIGURE 21 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 21. Medial view of right suspensorium of Capros aper, BMNH 2016.4.27.169-172, 51 mm SL Cartilage shown in dark grey. Abbreviations: ECTPT, ectopterygoid; HYOM, hyomandibular; IHY, interhyal; MESPT, mesopterygoid; METPT, metapterygoid; PAL, palatine; QUAD, quadrate; SYM, symplectic. Illustration by A.C. Gill.
FIGURE 18 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 18. Medial view of left lower jaw of Siganus spinus (Siganidae), ACG CS572, 61 mm SL: A) photo; B) camera lucida drawing. Abbreviations: ANGART, anguloarticular; DEN, dentary; DT, developing teeth; FT, functional teeth; MC, Meckel's cartilage; MT, migrating tooth; RETART, retroarticular. Images by A.C. Gill.
FIGURE 19 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 19. Lateral view of right (reversed) hyoid bar of Hapalogenys darwiniensis, paratype, CSIRO H.4069-12, 75.5 mm SL. Cartilage shown in dark grey. Abbreviations: ACH, anterior ceratohyal; BR, branchiostegal rays; DHH, dorsal hypohyal; PCH, posterior ceratohyal; VHH, ventral hypohyal. Illustration by A.C. Gill.
FIGURE 7. Capros aper, 2.3 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 7. Capros aper, 2.3 mm NL preflexion-stage larva, ZMUC P42224, Dana 3530I. Pigment omitted. Scale bar = 1 mm. Illustration by J.M. Leis and S.B. Leis.
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.