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.
12,237
datasets available to search
ShareScore release 0.9.0
Dataset results
12,237 results for “2019”
Figures 50-54 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 50-54 Brueeliakratochvili Balát, 1958, ex Motacillaflava Linnaeus, 1758 50 Male head, dorsal and ventral views 51 Male genitalia, dorsal view 52 Male mesosome, ventral view 53 Male paramere, dorsal view 54 Female subgenital plate and vulval margin, ventral view.
Figures 13-14 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 13-14 Brueeliabreueri Balát, 1955, ex Chlorischloris (Linnaeus, 1758). 13 Male habitus, dorsal and ventral views; 14 Female habitus, dorsal and ventral views.
Figures 57-61 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 57-61 Brueeliarosickyi Balát, 1955, ex Sylvianisoria (Bechstein, 1792) 57 Male head, dorsal and ventral views 58 Male genitalia, dorsal view 59 Male mesosome, ventral view 60 Male paramere, dorsal view 61 Female subgenital plate and vulval margin, ventral view.
Figures 34- 35 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 34- 35 Brueeliaconocephala (Blagoveshchensky, 1940) ex Sittaeuropaea (Linnaeus, 1758) 34 Male habitus, dorsal and ventral views 35 Female habitus, dorsal and ventral views.
Figures 17-21 from: Sendra A, Wagnell C (2019) The cave-dwelling dipluran (Diplura, Campodeidae) on the edge of the Last Glacial Maximum in Vancouver Island caves, North America (Canada). Subterranean Biology 29: 59-77. https://doi.org/10.3897/subtbiol.29.31467
Figures 17-21 Haplocampawagnelli Sendra, sp. n. 17 distal portion of femur and tibia from a metathoracic leg 18 tarsus 19 end of the tarsus and telotarsus 20 detail of posterior claw, lateral side 21 detail of posterior claw, lateral side.
Figures 22-26 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 22-26 Brueeliaglizi Balát, 1955, ex Fringillamontifringilla Linnaeus, 1758 22 Male head, dorsal and ventral views 23 Male genitalia, dorsal view, except mesosome which is distorted in specimen and here illustrated in dorso-lateral view 24 Male mesosome, ventro-lateral view 25 Male paramere, dorsal view 26 Female subgenital plate and vulval margin, ventral view.
Figures 20- 21 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 20- 21 Brueeliaglizi Balát, 1955, ex Fringillamontifringilla Linnaeus, 1758 20 Male habitus, dorsal and ventral views 21 Female habitus, dorsal and ventral views.
Figures 48- 49 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 48- 49 Brueeliakratochvili Balát, 1958, ex Motacillaflava Linnaeus, 1758 48 Male habitus, dorsal and ventral views 49 Female habitus, dorsal and ventral views.
Figures 1- 2 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 1- 2 Brueeliablagovescenskyi Balát, 1955, ex Emberizaschoeniclus (Linnaeus, 1758) 1 Male habitus, dorsal and ventral views 2 Female habitus, dorsal and ventral views.
Figures 27- 28 from: Gustafsson DR, Oslejskova L, Najer T, Sychra O, Zou F (2019) Redescriptions of thirteen species of chewing lice in the Brueelia-complex (Phthiraptera, Ischnocera, Philopteridae), with one new synonymy and a neotype designation for Nirmus lais Giebel, 1874. Deutsche Entomologische Zeitschrift 66(1): 17-39. https://doi.org/10.3897/dez.66.32423
Figures 27- 28 Brueeliakluzi Balát, 1955, ex Fringillacoelebs Linnaeus, 1758 27 Male habitus, dorsal and ventral views 28 Female habitus, dorsal and ventral views.
Figure 7 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 7 Mcvaughiapiauhiensis. A seasonally dry forests from Serra das Confusões, Piauí, Brazil B abaxial surface of a leaf C detail of epipetiolar stipules D inflorescence E rehydrated flower showing the stamens (white arrows= reduced stamens) and styles. A by S.E. Martins B–E by R.F. Almeida.
Figure 3 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 3 Leaf morphoanatomy of Mcvaughia species. A patterns of leaf glands distribution on the abaxial leaf surface of M.bahianaB patterns of leaf glands distribution on the abaxial leaf surface of M.piauhiensisC patterns of leaf glands distribution on the abaxial leaf surface of M.sergipanaD transverse section of leaf base showing the basilaminar pair of stalked glands (white arrows) E basilaminar leaf gland with a stalk (black arrow) in M.piauhiensisF basilaminar gland in M.sergipana showing a sessile position (SE= anatomical arrangement with secretory epidermis, SP= vascularized secretory parenchyma) G–H laminar glands on the apex of cleared leaves of M.sergipana and M.bahiana respectively, note the apical tooth (G) I sessile laminar glands in M.sergipanaJ stalked laminar gland in M.piauhiensisK–L transverse sections of the leaf blade; mesophyll with uniserial palisade-like parenchyma and spongy parenchyma composed by several or few layers in M.sergipana and M.bahiana, respectively; note the idioblast with druse crystals at the mesophyll (white arrow) and the stomata distribution at the abaxial leaf surface (black arrow) M–N adaxial epidermis surface of M.piauhiensis and M.sergipana, showing scars of malpighiaceous trichomes O abaxial epidermis surface of trichomes abundance in M.bahianaP–Q outline of the anticlinal epidermal cell walls: straight in M.sergipana (P) and sinuous in M.bahiana (Q). Laminar scale bars: 1 cm (A–C), 100 μm (D, F–K, N–O), 150 μm (E), 50 μm (L–M, P–Q).
Figure 1 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 1 Wood anatomy of Mcvaughiasergipana. A–B transverse sections: Growth rings marked by radially narrow fibers (arrowheads) and a discontinuous line of axial parenchyma (in B); vessels are narrow and abundant, arranged in radial rows of 4 or more cells; some solitary vessels present; parenchyma rare, paratracheal scanty or at the growth ring limits; heartwood vessels in the bottom with content C radial section: Rays 2–3 cells wide, non-storied; prismatic crystals present in ray cells (arrows); parenchyma with 3 cells per strand (arrowhead) D ray heterocellular with procumbent, square and upright cells mixed throughout the ray. Scale bars: 150 μm (A), 100 μm (B–C), 60 μm (D).
Figure 11 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 11 Distribution map of Mcvaughia: triangle – M.bahiana, circle – M.piauhiensis, and square – M.sergipana. Solid blue line in the center represents the São Francisco River today. Dotted blue line represents the past course of São Francisco River. Blue circle represents the São Francisco paleo lake. Light green – Atlantic Forest domain, dark green – Amazon Forest domain, orange – Cerrado domain, and yellow – Caatinga domain. AL – state of Alagoas, BA – state of Bahia, CE – state of Ceará, MA – state of Maranhão, PB – state of Paraíba, PE – state of Pernambuco, PI – state of Piauí, RN – state of Rio Grande do Norte, and SE – state of Sergipe.
Figure 5 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 5 Mcvaughiabahiana. A shrub habit B subshrub habit C inflorescence showing glandular bracts D inflorescence showing flowers in anthesis E inflorescence showing immature and mature fruits F detail of mature fruits G drupe indumentum H glabrescent drupe. A, D–H by W.R. Anderson B–C by I.R. Guesdon.
Figure 2 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 2 Secondary phloem of Mcvaughiasergipana. A–C Transverse section: A Phloem non-stratified, with scattered fiber-sclereids (arrows); Rays dilating slightly B Crystalliferous axial parenchyma arranged in diffuse-in-aggregate narrow bands (arrowhead) C Crystalliferous axial parenchyma with druse crystals, forming diffuse in aggregate bands, isolated fiber-sclereids present (arrowhead) D A ray 3 cells wide, fiber-sclereids and axial parenchyma in tangential section E Bands of crystalliferous parenchyma with druses evident also in radial section; Rays heterocellular mixed. Scale bars: 200 μm (A), 100 μm (B–C, E), 50 μm (D).
Figure 1 from: Kiew R, Lau K-H (2019) Senyumia granitica (Gesneriaceae) from Johor, Malaysia, the second species of Senyumia. PhytoKeys 117: 37-44. https://doi.org/10.3897/phytokeys.117.31560
Figure 1 Senyumiagranitica Kiew, sp. nov. A habit B Inflorescence showing partially resupinate flower C front view of a flower from Bukit Tukau population D front view of a flower from Bukit Reban Kambing population E side view of D; Senyumiaminutiflora (Ridl.) Kiew et al. F resupinate flower G side view of flower (upside down for comparison with E) H fruit of S.graniticaJTrigonalaeviceps on S.minutiflora, note full pollen baskets. (photographs by PT Ong).
Figure 9 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 9 Mcvaughiasergipana. A sandy dune where M.sergipana occurs B detail of epipetiolar stipules C detail of leaf venation patterns D abaxial surface of a leaf E inflorescence showing buds and flowers F detail of glandular bracts G floral bud H flower in frontal view I fruit in side view. Photos by R.F. Almeida.
Figure 4 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 4 Reproductive morphoanatomy of Mcvaughia species. A inflorescence during development, showing a bracteole gland (BG) and Sepal glands (SG) B ten sepal glands encircling the calyx C Petal glands (PG) along the margin of posterior petal D–F transverse section of bracteole glands in M.sergipana, M.bahiana and M.piauhiensis, respectively G anatomical arrangement of bracteole gland, with a palisade-like secretory epidermis (SE) and secretory parenchyma (SP) H–I transverse section of floral bud and anthesis flower in Mcvaughiabahiana and M.sergipana; calyx gland pair displaced at the anterior sepal J calyx gland structure, showing a secretory epidermis (SE) and vascularized secretory parenchyma (SP) K–L petal glands on the margin of petals in M.sergipana and M.bahiana respectively M–N detail of the petal glands at the apex of the petal limb in M.sergipana, cleared and in SEM image O–Q petal glands positioned at the base, M.bahiana on SEM image, M.bahiana and M.piauhiensis cleared R–T conspicuous and stalked petal glands at the base of M.sergipana, in SEM image, cleared and longitudinal section. Scale bars: 200 μm (D), 150 μm (E–F), 50 μm (G), 500 μm (H–I), 100 μm (J, P–S), 300 μm (L–M), 200 μm (N, T).
Figure 3 from: Weiner WM, Xie Z, Li Y, Sun X (2019) Ceratophysella species from mushrooms in China (Collembola, Hypogastruridae). ZooKeys 822: 67-77. https://doi.org/10.3897/zookeys.822.30880
Figure 3 Ceratophysellaskarzynskii sp. n. A tibiotarsus and claw III B dens and mucro C abd. V and VI D set of dens chaetae. Scale bars: 0.01 mm.
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.