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Figure 11 in First results of a faunistic survey on the Orthoptera of Jadovnik Mountain, southwestern Serbia, with data on the calling songs of some bush cricket species
Figure 11. SEM photographs of the stridulatory files: (A) Poecilimon pseudornatus, Sopotnica Ra; (B) Poecilimon pseudornatus, Ogoreljača–Mali Jadovnik (roadside).
Figure 4 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 4. Cumulative plot showing the number of new syllable types produced by 20 Daurian Redstart males against the nth bird sampled in South Korea. The number of the new syllable types leveled off at approximately the 15th male sampled; the equation shown is for the curve-fit.
Figure 5 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 5. Cumulative number of syllable types per each song part produced by 20 Daurian Redstart males against the nth bird sampled in South Korea.
Figure 3 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure 3. Cumulative plot showing the number of syllable types produced by 20 Daurian Redstart males against the nth song sampled. Most of the songs reached the peak syllable types at approximately the 18th song. A1 to E4 is the ID of each individual.
Figure S1 in The song structure and repertoire size of Daurian Redstarts (Phoenicurus auroreus) in South Korea
Figure S1. Syllable types in whistle, subsyllable, and syllable parts of 400 songs of 20 individuals from five population samples in 2015 and 2016 in South Korea.
Figure 3 in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 3. General view of the colony Zoothamnium sinense Song, 1991 (original, in vivo), scale bar: 250 µm.
Figure 4. Zoothamnium sinense Song, 1991. A, C in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 4. Zoothamnium sinense Song, 1991. A, C – original, in vivo, scale bar: 35 µm; В – modified from Ji et al., 2006, scale bar: 20 µm.
Fig. 3 in Exo-erythrocytic development of Leucocytozoon parasites (Haemosporida, Leucocytozoidae) in song thrushes Turdus philomelos
Fig. 3. Tissue and blood stages of Leucocytozoon parasites in naturally infected song thrushes Turdus philomelos (individual no. 4, cytochrome b lineage lSTUR1), found in hematoxylin-eosin (H&E) stained (a-g, i), chromogenic in situ hybridization (CISH) treated (h and inserts a-c, e, i) histological sections. Early (a), advanced (b, c) and mature (d) meronts in the kidneys. Megalomeront-like structure (e-h) located close to a heart blood vessel (white asterisk) within the fat tissue (black asterisk). Leucocytozoon gametocytes in the kidneys (i). Simple black arrowheads: meronts. Simple white arrowhead: cytomeres (visible as darker stained nuclei surrounded by lighter stained clefts). Black triangle arrowhead: megalomeront-like structure. Short black triangle arrow: capsule-like wall. Short white triangle arrow: host cell nucleus in the capsule-like wall. Short simple white arrows: nuclei of infected host cells. Simple thin black arrows: gametocytes. Scale bars 20 μm, unless indicated otherwise.
Fig. 2 in Exo-erythrocytic development of Leucocytozoon parasites (Haemosporida, Leucocytozoidae) in song thrushes Turdus philomelos
Fig. 2. Tissue stages of Leucocytozoon parasites in naturally infected song thrushes Turdus philomelos, found in hematoxylin-eosin (H&E) stained (a, b, e, f) and chromogenic in situ hybridization (CISH) treated (insert in b, and c, d) histological sections. Early meronts in the kidneys of individual no. 1 (cytochrome b lineage lTUPHI14) (a), and advanced meronts in the kidneys of individual no. 2 (lSTUR1) (b) and no. 5 (co-infection of lSTUR1 and lTUPHI13) (e, f). Meronts labelled by a Leucocytozoon-specific (Leuco18S) probe in the kidneys (insert b), and lungs of individual no. 2 (lSTUR1) (c) and individual no. 3 (lSTUR1) (d). Tissue stage developing in the Bowman capsule of a renal corpuscle (e). Leucocytozoon blood stage labelled by a Leucocytozoon-specific probe (c). Simple black arrowheads: meronts. Simple white arrowheads: cytomeres (visible as darker stained nuclei surrounded by lighter staining clefts). Short simple black arrow: nucleus of Leucocytozoon blood stage. Scale bars 20 μm.
Fig. 1 in Exo-erythrocytic development of Leucocytozoon parasites (Haemosporida, Leucocytozoidae) in song thrushes Turdus philomelos
Fig. 1. Mature gametocytes of Leucocytozoon dubreuili in roundish host cells from the blood of a song thrush Turdus philomelos (individual no. 1, cytochrome b lineage lTUPHI14). Macrogametocyte (a). Microgametocyte (b). Short simple white arrows: nuclei of infected host cells. Short simple black arrow: parasite nucleus. Long simple white arrows: vacuoles. Long simple black arrow: volutin granules (small purplish dots). Methanol-fixed and Giemsa-stained. Scale bar 10 μm.
Character Networks of 'A Song of Ice and Fire' Adaptations Across Media
<p><strong>Description. </strong>This work aims at comparing three crossmedia adaptations of the same story: George R. R. Martin’s <em>A Song of Ice an Fire</em> original novels, the comics directly adapted from this series, and the <em>Game of Throne</em> TV show. To perform our analysis, we used two representations of these stories: textual vs. graph-based. The textual one corresponds to summaries, whereas the graphs are character networks, representing the interactions between characters. We performed a descriptive analysis of the three adaptations, and tackle a task consisting in automatically aligning the three stories.</p> <p>This dataset contains the input files used by our scripts (various versions of the character networks) as well as the files produced during the processing.</p> <ul> <li>The archives starting with `nets_` correspond to the network files used as input during processing.</li> <li>Those starting with `out_` are the files (mainly stats and plots) produced by our scripts.</li> </ul> <p>The networks are available in several versions, using the `graphml` format:</p> <ul> <li>Folder `cumul`: cumulative networks, i.e. dynamic networks that grow from the beginning to the end of the story. The very last network corresponds to the <em>static</em> network, i.e. the network representing the whole timeline.</li> <li>Folder `instant`: also a dynamic network, but this time each instant is not considered as an increment. Each `graphml` file only focuses on a specific temporal subdivision of the story.</li> </ul> <p>The temporal subdivisions depend on the considered medium:</p> <ul> <li>Novels: only <em>chapter</em>.</li> <li>Comics: <em>chapter</em> or <em>scene</em>.</li> <li>TV show: <em>episode</em>, <em>block</em> or <em>scene</em>.</li> </ul> <p>TV show blocks were defined <em>ad hoc</em> to get a subdivision larger than a scene but smaller than a whole episode. We experimented with two versions: blocs based on the location persistence vs. character similarity.</p> <p><strong>Software. </strong>The scripts are publicly available online: <a href="https://github.com/CompNet/Sachan">https://github.com/CompNet/Sachan</a></p> <p><strong>References. </strong>This work was published in the following article:</p> <ul> <li> <div> <div>A. Amalvy, M. Janickyj, S. Mannion, P. MacCarron, and V. Labatut, “Interconnected Kingdoms: Comparing ‘A Song of Ice and Fire ́Crossmedia Adaptations Using Complex Networks,” <em>Social Network Analysis and Mining</em>, vol. 14, p. 199, 2024. DOI: <a href="https://doi.org/10.1007/s13278-024-01365-z">10.1007/s13278-024-01365-z</a> ⟨<a href="https://hal.science/hal-04722579">hal-04722579</a>⟩</div> </div> </li> </ul> <p><strong>Citation. </strong>If you use these scripts, please cite the above article:</p> <pre><code>@Article{Amalvy2024c, author = {Amalvy, Arthur and Janickyj, Madeleine and Mannion, Shane and MacCarron, Pádraig and Labatut, Vincent}, title = {Interconnected Kingdoms: Comparing `A Song of Ice and Fire' Crossmedia Adaptations Using Complex Networks}, journal = {Social Network Analysis and Mining}, year = {2024}, volume = {14}, pages = {199}, doi = {10.1007/s13278-024-01365-z}, }</code><br><br></pre>
Linked collectors and determiners for: Crickets of the subfamily Eneopterinae (Orthoptera: Grylloidea) from Sandakan, Sabah: one new species and calling songs of a sympatric species.
Natural history specimen data linked to collectors and determiners held within, "Crickets of the subfamily Eneopterinae (Orthoptera: Grylloidea) from Sandakan, Sabah: one new species and calling songs of a sympatric species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/1e87ced1-1631-463d-92d4-508d30dbbc48">https://bionomia.net/dataset/1e87ced1-1631-463d-92d4-508d30dbbc48</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/1e87ced1-1631-463d-92d4-508d30dbbc48">https://gbif.org/dataset/1e87ced1-1631-463d-92d4-508d30dbbc48</a>. Formatted as a Frictionless Data package.
Figure 1 in Stridulation in Aphodius dung beetles: Songs and morphology of stridulatory organs in North American Aphodius species (Scarabaeidae)
Figure 1. The abdomino-alary stridulatory organ of Aphodius sp. The plectrum is on the first abdominal segment (a) and the file is on the underside of the hindwing (b).
Figure 2 in Stridulation in Aphodius dung beetles: Songs and morphology of stridulatory organs in North American Aphodius species (Scarabaeidae)
Figure 2. Sonagrams with duration of 30 s (a) and 1 s (b) of A. pectoralis, A. granarius, A. rainieri and A. sigmoideus. Spectrograms show the frequency during 0.5 s (c).
Figure 4 in Stridulation in Aphodius dung beetles: Songs and morphology of stridulatory organs in North American Aphodius species (Scarabaeidae)
Figure 4. SEMs of the stridulatory organ. (a) Plectrum of A. pectoralis; (b) file of A. pectoralis; (c) plectrum of A. granarius; (d) file of A. granarius; (e) plectrum of A. rainieri; (f) file of A. rainieri; (g) plectrum of A. sigmoideus; (h) file of A. sigmoideus.
Figure 6 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 6. Scatterplot of the first two roots of a discriminant function analysis of nine song features (see text) of Cc5, C. zastrowi, C. lucasina, C. mediterranea and C. agilis. Each data point represents a single individual, coded by taxon.
Figure 2 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 2. Oscillograms (volts on y-axis) and sonagrams (Hertz on y-axis) of typical solo (non-dueting) vibrational songs. (A) Cc5, five volleys or shortest repeated units (SRUs); (B) Cc5, detail of a single volley/SRU; (C) C. zastrowi, five volleys or shortest repeated units (SRUs), drawn to same time scale as A. Song features discussed in the text are labeled.
Figure 4 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 4. Two key morphological features of lacewing taxa. (A) Fore wing of Cc5 (above) and C. zastrowi (beneath). Note the contrasting perpendicular versus oblique orientation of the Rs-M crossvein in the two taxa. (B) Lateral view of the lip/chin of sternite 8+9 of the male abdominal apex. Letters A–G represent landmarks used to determine relative shapes and sizes of the lip and chin. All specimens of both Cc5 and C. zastrowi showed line segment AB.BC, indicating a relatively broad, protruding lip.
Figure 3 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 3. Oscillograms comparing typical heterosexual duets, drawn to the same time scale. (A) Cc5; (B) C. zastrowi. Note the presence of occasional transient volley breaks (arrows) in the songs of both taxa.
Figure 1 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 1. Map of Africa and Middle East showing collecting localities of Cc5, C. zastrowi and specimens closely resembling those taxa.
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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.