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.
1,112
datasets available to search
ShareScore release 0.9.0
Dataset results
1,112 results for “canals”
Figures 113–122. Reproductive organs. 113–114. Priocera hypocrita. 113 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 113–122. Reproductive organs. 113–114. Priocera hypocrita. 113) Male. 114) female. 115–118. Females. 115) Priocera sp. 116) Priocera variegata. 117) Stigmatium sp. 118) Stigmatium gilberti. 119–120. Thanasimus dubius. 119) male. 120) female. 121–122) Thanasimus formicarius males.
Figures 96–105. Reproductive organs. 96–101. Omadius females. 96 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 96–105. Reproductive organs. 96–101. Omadius females. 96) sp.k. 97) sp. l. 98) sp. m 99) sp. n. 100) sp. o. 101) sp. p. 102–105. Opilo taeniatus 102) male. 103) female. 104–105) Males.
Figures 84–95. Omadius reproductive organs. 84–93. Males. 84 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 84–95. Omadius reproductive organs. 84–93. Males. 84) sp.a. 85) sp. b. 86) sp. c. 87) sp. d. 88) sp. e. 89) sp. f. 90) sp. g. 91) sp. h. 92) sp. i. 93) sp. j. 94–95. Females. 94) sp. j. 95) sp. h.
Figures 73–83. Alimentary canals and reproductive organs. 73–75 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 73–83. Alimentary canals and reproductive organs. 73–75. Eunatalis sp. a. 73) Alimentary canal. 74) Reproductive organs, male. 75) Reproductive organs, female. 76–77. Eunatalis sp. b. 76) Reproductive organs, female. 77) Reproductive organs, male. 78) Metademius reproductive organs, female. 79–80. Omadius semicarinatus. 79) Reproductive organs, male. 80) Reproductive organs, female. 81–83. Neoscrobiger patricius. 81) Reproductive organs, male. 82) Reproductive organs, female. 83) Alimentary canal.
Figures 60–72. Reproductive organs. 60–64. Eleale, males. 60 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 60–72. Reproductive organs. 60–64. Eleale, males. 60) sp. a. 61) sp. b. 62) sp. c. 63) sp. d. 64) sp. e. 65–69. Eleale females. 65) sp.f. 66) sp. d. 67) sp. c. 68) sp. g. 69) sp. h. 70–72. Epiclines basalis. 70) male. 71) female. 72) male.
Figures 52–59. Reproductive organs and alimentary canals. 52–54, 56, 58, 59. Reproductive organs. 52 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 52–59. Reproductive organs and alimentary canals. 52–54, 56, 58, 59. Reproductive organs. 52) Cardiostychus gabonicus, female. 53–54. Cardiostychus sp. 53) male 54) female. 55–56. Chiloclerus mimus. 55) Alimentary canal. 56) Reproductive organs, male. 57–59. Clerus mutillarius. 57) Alimentary canal. 58) Reproductive organs, female. 59) Reproductive organs, male.
Figures 45–51. Reproductive organs and alimentary canals. 45–47, 49, 51. Reproductive organs. 45–46. Caeston concinus. 45 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 45–51. Reproductive organs and alimentary canals. 45–47, 49, 51. Reproductive organs. 45–46. Caeston concinus. 45) male. 46) female. 47) Caeston contractus, female. 48–49. Calendyma chilensis. 48) Alimentary canal. 49) Reproductive organs, female. 50–51. Cardiostychus gabonicus. 50) Alimentary canal. 51) reproductive organs, male.
Figures 1–12. Alimentary canals and reproductive organs. 1–3. Alimentary canals. 1 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 1–12. Alimentary canals and reproductive organs. 1–3. Alimentary canals. 1) Somatochaetus quadraticollis. 2) Metaxina ornata. 3) Ababa sp. 4–12. Reproductive organs. 4) Callimerus sp., female. 5–6. Eurymetopum maculatum, 5) male, 6) female. 7–12. Eurymetopum spp., 7) sp. a., male. 8) sp. b., male. 9) sp. c., female. 10) sp. d., female. 11) sp. e., female. 12). Isohydnocera aegra, male.
Figures 36–44. Reproductive organs. 36 in Morphologic studies of the alimentary canal and internal reproductive organs of the Chaetosomatidae and the Cleridae (Coleoptera: Cleroidea) with comparative morphology and taxonomic analyses
Figures 36–44. Reproductive organs. 36) Phyllobaenus sp., female. 37) Aulicus femoralis, male. 38) Aulicus nigriventris, female. 39) Wolcottia sobrina, female. 40–41. Axina conspicua. 40) male. 41) female. 42) Axina bifasciata, male. 43) Axina plagiata, male. 44) Axina parcepunctata, female.
Fig. 1 in The Singscore: a macroinvertebrate biotic index for assessing the health of Singapore's streams and canals
Fig. 1. Map of Singapore showing the 47 study sites (black circles) located in 33 concrete canals, and 14 forested streams. Note that all forested streams were located within the Central Catchment Nature Reserve (CCNR; dark grey area in centre of the map). Inset shows forested study sites within the CCNR.
Fig. 2 in The Singscore: a macroinvertebrate biotic index for assessing the health of Singapore's streams and canals
Fig. 2. Partial canonical correspondence analysis (pCCA) ordination showing differences in macroinvertebrate community composition in the 33 urban canals (open circles) and the 14 reference streams (closed triangles). The main environmental drivers (pH and copper) of community dissimilarity are depicted as solid arrows.
Fig. 3 in The Singscore: a macroinvertebrate biotic index for assessing the health of Singapore's streams and canals
Fig. 3. Non-metric multidimensional scaling (NMDS) ordination based on a Bray-Curtis matrix of dissimilarities calculated from presence-absence data illustrating compositional differences in macroinvertebrate communities among the sites. The NMDS gave a good representation of actual community dissimilarities (2-dimensional stress = 0.16) and ANOSIM separated the sites into four relatively distinct groups (ANOSIM, Global R = 0.769, P = 0.001), interpreted as likely water-quality categories (poor: closed circle; fair: open square; good: closed triangle; excellent: open circle). Axes are scaled identically so that sites closest together are more similar in macroinvertebrate community composition than those further apart.
FIG. 7. — A, B, Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 7. — A, B, Janstockia phallusiella n. gen., n. sp.; A, leg 1; B, leg 2; C, Ophioseides cardiocephalus Hesse, 1864, leg 1. Scale bars: 50 μm.
FIG. 5. — Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 5. — Janstockia phallusiella n. gen., n. sp.; A, urosome, ventral view; B, copulatory pore and paired sperm ducts, with blind projections; C, cluster of setae representing incorporated caudal rami, showing setular ornamentation, dorsal view; D, urosome, dorsal view; E, mandibular palp; F, maxillule; G, maxilliped; H, tip of maxilliped. Scale bars: A, D, 200 μm; B, C, F, H, 25 μm; E, G, 50 μm.
FIG. 4. — Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 4. — Janstockia phallusiella n. gen., n. sp., scanning electron micrographs; A, mandibular palp, ventral view in situ; B, maxillule, ventral view in situ; C, hirsute lobes of maxillule; D, maxilliped. Scale bars: A-C, 10 μm; D, 20 μm.
FIG. 1. — Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 1. — Janstockia phallusiella n. gen., n. sp.; A, habitus of paratype (MNHN-Cp2178), lateral view; B, habitus of holotype (MNHN-Cp2177), ventral view; C, habitus of holotype, dorsal view showing lateral expansions of first pedigerous somite (arrow). Scale bars: A, 1.0 mm; B, C, 0.5 mm.
FIG. 9 in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 9. — Schematic of leg 2 of Janstockia phallusiella n. gen., n. sp. Abbreviations: ba, basis; en1-3, endopodal segments 1 to 3; ex1-3, exopodal segments 1 to 3; ics, intercoxal sclerite; os, outer basal seta.
FIG. 6. — Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 6. — Janstockia phallusiella n. gen., n. sp., scanning electron micrographs; A, leg 1, anteroventral; B, detail of leg 1 exopod; C, rami of leg 2; D, leg 4; E, detail of leg 3 rami; F, detail of leg 4 rami. Scale bars: A, 20 μm; B, C, E, F, 10 μm; D, 50 μm.
FIG. 8 in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 8. — Ophioseides cardiocephalus Hesse, 1864; A, antennule; B, tip of antennule showing setal elements; C, antenna; D, detail of antennal endopod, showing claw and accessory setae; E, oral appendages in situ. Abbreviations: mn, mandible; mx, maxilla; mxl, maxillule. Scale bars: A, C-E, 50 μm; B, 25 μm.
FIG. 3. — Janstockia phallusiella n. gen., n in A new genus of notodelphyid copepod (Crustacea, Copepoda, Cyclopoida) from a compound ascidian host collected in the Suez Canal
FIG. 3. — Janstockia phallusiella n. gen., n. sp., scanning electron micrographs; A, cephalosome and anterior part of trunk, ventral view; B, rostrum, labrum and oral area, ventral view; C, detail of trunk surface showing integumental ornamentation; D, genital openings, ventral view. Scale bars: A, 200 μm; B, 100 μm; C, 10 mm; D, 50 μm.
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.