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.
2,358
datasets available to search
ShareScore release 0.7.1
Dataset results
2,358 results for “wing”
FIG. 5 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 5. Morphological characters of Greenagraecia cooloola gen., sp. nov. A, adult male. B, adult female. C, frons, female.
MAP 2 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
MAP 2. Known distribution of two agraeciine species. - Greenagraecia cooloola gen. et sp. nov.yGeoffagraecia gwinganna gen. et sp. nov.
FIG. 4 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 4. Morphological characters of Greenagraecia attenuata gen., sp. nov. A, tip of abdomen, male. B, same, male, left cercus removed; note tenth tergite. C, male left cercus, dorsal view. D, male left cercus, posterior view. E, male left cercus, internal view. F, male left cercus, note small hook. G, female subgenital plate. H, female subgenital plate, lateral view. I, female subgenital plate pocket or opening at base. J, male phallic complex. K, male phallic complex, Cape Tribulation. L, head, pronotum brown morph.
FIG. 8 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 8. Morphological characters of Geoffagraecia gwinganna gen., sp. nov. A, frons, holotype male. B, fastigium of vertex and antennal segments, male. C, foreleg, holotype male. D, hind femur, note spine and colour, holotype male. E, male left cercus, dorsal view. F, male left cercus, internal view. G, tegmen, holotype male. H, tip of abdomen, holotype male. I, subgenital plate, holotype male. J, male phallic complex, holotype. K, odd tarsal development, see text. L, subgenital plate, female paratopotype. M, same, Big Bend. N, ovipositor, paratopotype.
FIG. 11 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 11. Morphological characters of Barbaragraecia richardsoni gen., sp. nov. A, adult female, Kuranda. B, head and pronotum adult female, note structure of pronotum over thoracic auditory opening. C, adult male Kuranda. D, adult male from Mt Lewis with macerated prey, probably a caterpillar. E, adult male in defensive posture.
FIG. 7 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 7. Morphological characters of Geoffagraecia gwinganna gen., sp. nov. A, male. B, male, note abdominal colour. C, ovipositor and lateral view female abdomen.
FIG. 6 in Studies in Australian Tettigoniidae: New Fully-winged Agraeciini From Northeastern Australia (Orthoptera: Tettigoniidae; Conocephalinae; Agraeciini)
FIG. 6. Morphological characters of Greenagraecia cooloola gen., sp. nov. A, frons holotype. B, fastigium of vertex, male. C, pronotum, male. D, pronotum, lateral view, male. E, fore tibia holotype male, note margins of auditory foramina and colour spots. F, middle tibia, holotype male. G, tegmen and wing, male. H, left male cercus, dorsal view. I, same internal view. J, same, internal view, note minute teeth. K, same ventral view. L, tip of abdomen, dorsal view, female. M, subgenital plate, female. N, male phallic complex.
FIGURES1–7. Dendrothrips karnyi, female (1) Body; (2); Meso & metathorax (3)Head & pronotum; (4)Antenna; (5)Abdominal tergites IV–VII; (6) Abdominal sternites II–V; (7)Fore wing. in --First--description --of--the--male-- of--Dendrothrips karnyi (Thysanoptera,--Thripidae)-from-- Iran
FIGURES1–7. Dendrothrips karnyi, female (1) Body; (2); Meso & metathorax (3)Head & pronotum; (4)Antenna; (5)Abdominal tergites IV–VII; (6) Abdominal sternites II–V; (7)Fore wing.
FIGURES 27–34 Wing patterns. 27. Rhopaltriplasia anamilleta Diakonoff, 1973 28 in First report on the Olethreutini (Lepidoptera: Tortricidae: Olethreutinae) of Lao PDR with descriptions of two new species
FIGURES 27–34 Wing patterns. 27. Rhopaltriplasia anamilleta Diakonoff, 1973 28. Sisona albitibiana (Snellen, 1902) 29. Sorolopha archimedias (Meyrick, 1912) 30. Sorolopha argyropa Diakonoff, 1973 31. Sorolopha cyclotoma Lower, 1901 32. Statherotis discana (Felder & Rogenhofer, 1875) 33. Statherotis leucaspis (Meyrick, 1902) 34. Sycacantha inodes (Meyrick, 1911).
FIGURES 17–26. Wing patterns. 17. Lobesia genialis Meyrick, 1912 18. Lobesia kurokoi Bae, 1995 19. Lobesia lithogonia Diakonoff, 1954 20. Lobesia moriutii Bae, 1995 21. Megalota fallax Meyrick, 1909 22. Megalota vera Diakonoff, 1966 23. Neopotamia divisa Walsingham, 1900 24. Ophiorrhabda cellifera Meyrick, 1912 25 in First report on the Olethreutini (Lepidoptera: Tortricidae: Olethreutinae) of Lao PDR with descriptions of two new species
FIGURES 17–26. Wing patterns. 17. Lobesia genialis Meyrick, 1912 18. Lobesia kurokoi Bae, 1995 19. Lobesia lithogonia Diakonoff, 1954 20. Lobesia moriutii Bae, 1995 21. Megalota fallax Meyrick, 1909 22. Megalota vera Diakonoff, 1966 23. Neopotamia divisa Walsingham, 1900 24. Ophiorrhabda cellifera Meyrick, 1912 25. Ophiorrhabda mormopa (Meyrick, 1906) 26. Ophiorrhabda philocompsa (Meyrick, 1921).
FIGURES 7–16. Wing patterns. 7. Diakonoffiana laosensis, n in First report on the Olethreutini (Lepidoptera: Tortricidae: Olethreutinae) of Lao PDR with descriptions of two new species
FIGURES 7–16. Wing patterns. 7. Diakonoffiana laosensis, n.sp. (holotype male) 8. Do. n.sp. (paratype female) 9. Dicephalarcha herbosa (Meyrick, 1909) 10. Dudua aprobola (Meyrick, 1886) 11. Dudua charadraea (Meyrick, 1909) 12. Dudua tetanota Meyrick, 1909 13. Gatesclarkeana idia Diakonoff, 1973 14. Hedya iophaea Meyrick, 1912 15. Lobesia acicula, n.sp. (holotype male) 16. Lobesia aeolopa Meyrick, 1907.
FIGURE 4. Hind wings, dorsal view. A–C in Caliroa slug sawflies of Japan (Hymenoptera, Tenthredinidae)
FIGURE 4. Hind wings, dorsal view. A–C, Caliroa cerasi: A, female, Sapporo; B, female, Shimizu; C, male, Finland. D, C. bibaiensis, female, holotype. E, F, C. oishii: E, female, holotype or paratopotype; F, male, Shintoku. G, H, C. ibukii: G, female, holotype; H, male, paratype. I–K, C. vaccini: I, female, paratype; J, female, holotype or paratype; K, male, paratype. L, C. ouensis, female, holotype. M, C. aizankei, female, holotype. N–P, C. staphyleae: N, female, lectotype; O, female, Nakagawa; P, male, paralectotype. Q, R, C. zelkovae: Q, female, lectotype; R, male, Hobara. S, C. matsumotonis, male, Korea. T, C. nire, female, holotype. A, C, D, F, J, K, reversed.
Wing morphological responses to latitude and colonisation in a range expanding butterfly
<p>Images of male Speckled Wood butterfly (<em>Pararge aegeria</em>) wings that were collected (during 2016-2018) across a recently expanded range in mainland Britain. The wings were used to study changes in morphology (size and shape) and colour with colonisation history, latitude and temperature.</p> <p>Images were taken by Evelyn D. Taylor-Cox and Claire Williams in the Lepidoptera Ecological Genetics Group at the Univeristy of Liverpool, under the supervision of Ilik J. Saccheri. </p> <p> </p> <p>Files included:</p> <ol> <li>Parage_aegeria_RAW.zip <ul> <li>Nikon raw camera images (.NEF) with ColorGauge Micro Target (Image Science Associates) colour calibration grid</li> </ul> </li> <li>Raw_example.NEF <ul> <li>Example raw image for preview</li> </ul> </li> <li>Pararge_aegeria_landmarks_jpeg.zip <ul> <li>Selected wings for landmarking and associated landmark coordinate files (.TPS)</li> <li>These images have been calibrated and cropped to either the left forewing or hindwing (dorsal surfaces only)</li> </ul> </li> <li>Pararge_aegeria_colour_png.zip <ul> <li>Selected wings for colour analysis (.png)</li> <li>These images have been calibrated and cropped to either the left forewing or hindwing (both ventral and dorsal)</li> </ul> </li> <li>Calib_cropped_FW_D_example.png <ul> <li>Example cropped and calibrated forewing image, dorsal surface (in .png format)</li> </ul> </li> </ol> <p> </p> <p>Nomenculture (for 2017/18 samples, principle collector EDTC):</p> <ul> <li>PA_*_XX: site number (*) and site code (XX)</li> <li>_##: within site sample number (##)</li> <li>_V or _D: ventral or dorsal surface</li> </ul> <p>Nomenculture (for 2016/7 samples, principle collector CM):</p> <ul> <li>PA_**M#: site reference(**)_Male (M)_within site number(#)</li> <li>_V or _D: ventral or dorsal surface</li> </ul> <p> </p> <p>This work was funded by the Natural Environment Research Council (NERC ACCE: studentship to EDTC, grant number NE/L002450/1, NE/N015711/1 awarded to IJS and NE/N015797/1 JKH).</p> <p> </p> <p><strong>Please contact Ilik J. Saccheri (saccheri@liverpool.ac.uk) or Evelyn D. Taylor-Cox (e.taylorcox@hotmail.co.uk) for requests.</strong></p> <p> </p>
FIG. 5 in Bat diversity in the Simandou Mountain Range of Guinea, with the description of a new white-winged vespertilionid
FIG. 5. Dorsal and ventral view of a live-captured N. tenuipinnis from Liberia. Note the dark dorsal fur (Photographs by A. Monadjem)
FIG. 6 in Bat diversity in the Simandou Mountain Range of Guinea, with the description of a new white-winged vespertilionid
FIG. 6. Outlines of the left tragus in N. rendalli (left), N. tenuipinnis (middle; both redrawn after Rosevear 1965), and N. isabella sp. nov. (holotype)
FIGURE 2 in Discrimination of Uranotaenia species (Diptera: Culicidae) from Madagascar based on morphology and wing morphometric traits
FIGURE 2. Twelve landmarks on the wing of the Uranotaenia specimens used in the morphometric analyses.
FIGURE 5 in Discrimination of Uranotaenia species (Diptera: Culicidae) from Madagascar based on morphology and wing morphometric traits
FIGURE 5. Variation of the centroid size of the wing for Uranotaenia sp1 from the Anorana forest (1) and the Maromizaha forest (2). Each box shows the group of median values separating the 10th and 90th quartiles.
Identification of Megaselia (Diptera: Phoridae) species using wing vein landmarking
<p>A semi-automated identification system using wing venation is described for the large, taxonomically challenging genus <i>Megaselia</i> Rondani (Diptera: Phoridae). Wing photographs make two-dimensional images that can be landmarked and analyzed to produce transformed (standardized) x-y coordinates, and are well-suited for a semi-automated approach. We landmarked wing photographs of individuals of 108 specimens of <i>Megaselia</i> from the ZADBI (Zurqui All Diptera Biodiversity Inventory) project, as well as 284 specimens of <i>Megaselia</i> from the Los Angeles based BioSCAN (Biodiversity Science: City and Nature) project and ran them against libraries of one specimen of each species of the fauna from each site, respectively. Accuracy was about 52-67% for the first identification, with 86-95% of correct identifications in the top 5 candidates list. Expanding the library to include all identified specimens raised the likelihood that the first identification was correct to 93-96% of specimens, with 97-98% correct identifications in the top 5 list. Incorporating major body color (dark brown versus yellowish) to the identification system increased accuracy to 100% for the ZADBI specimens; other, easily-seen characters were used for problematic LA specimens. We suggest that a wing photograph be included in all <i>Megaselia</i> species descriptions to allow this semiautomation of identification based on morphology, and further that this system could provide a bridge to DNA-based species descriptions from old holotypes in collections.</p>
Wing: A suitable non-lethal tissue type for repeatable and rapid telomere length estimates in bats
Telomeres are used increasingly in ecology and evolution as biomarkers for ageing and environmental stress, and are typically measured from DNA extracted from non-lethally sampled blood. However, obtaining blood is not always possible in field conditions and only limited amounts can be taken from small mammals, such as bats, which moreover lack nucleated red blood cells and hence yield relatively low amounts of DNA. As telomere length can vary within species according to age and tissue, it is important to determine which tissues serve best as a representation of the organism as a whole. Here, we investigated whether wing tissue biopsies, a rapid and relatively non-invasive tissue collection method, could serve as a proxy for other tissues when measuring relative telomere length (rTL) in the Egyptian fruit bat (Rousettus aegyptiacus). Telomeres were measured from blood, brain, heart, kidney, liver lung, muscle and wing, and multiple wing biopsies were taken from the same individuals to determine intra-individual repeatability of rTL measured by using qPCR. Wing rTL correlated with rTL estimates from most tissues apart from blood. Blood rTL was not significantly correlated with rTL from any other tissue. Blood and muscle rTL were significantly longer compared with other tissues, while lung displayed the shortest rTLs. Individual repeatability of rTL measures from wing tissue was high (>76%). Here we show the relationships between tissue telomere dynamics for the first time in a bat, and our results provide support for the use of wing tissue for rTL measurements.
Overlap in the wing shape of migratory, nomadic and sedentary grass parrots
Bird wing shape is highly correlated with mobility, and vagile species have more pointed wing tips than sedentary ones. Most studies of bird wing shape are biased to the northern hemisphere, and consider only two migratory syndromes (north-south migrants or sedentary species). There are major gaps in knowledge about the wing shapes of different taxa with other movement strategies (e.g. nomads) in the southern hemisphere. Parrots are a prominent southern hemisphere bird order with complex movement patterns, but their wing shapes are mostly unstudied. We test whether three metrics of wing shape of grass parrots (Neophema and Neopsephotus spp.) correspond to their purported migration syndromes (and other factors). We show that two strongly migratory grass parrots and an arid-adapted nomad had pointed wings, with flight feather longer distally and shorter proximally. However, purportedly sedentary species overlapped extensively with migrants and nomads in all aspects of wing shape, and taxonomic relationships, purported migratory syndromes and ecological barriers did not explain the variation we recorded. The most distantly related species (Neopsephotus) had most dissimilar wing shape to the others, but broadly conformed to the expectations of long pointed wings of a nomad. Why purportedly sedentary grass parrots had unexpectedly pointed wings is unclear. We propose the hypothesis that this wing shape may persist in sedentary populations if individuals experience strong but intermittent selection to disperse when environmental conditions are poor. If pointed wings are not costly during good times when individuals are sedentary, this wing shape may persist in populations as a 'back up' in bad times. Our study highlights the interesting migration patterns in the southern hemisphere that remain largely unstudied. Wing shape offers an interesting way to identify potentially undiscovered capacity for movement in data deficient species, which may also have implications for conservation.
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.