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Figure 6. A–C in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 6. A–C, Comasarcophaga texana: A, distiphallus, lateral; B, distiphallus, anterior; C, styli, anterior. D–F, Cistudinomyia cistudinis: D, distiphallus, lateral; E, distiphallus, anterior; F, styli anterior. Abbreviations: J, juxta; LS, lateral stylus; MS, median stylus; PT, phallic tube; V, vesica.
Figure 5. A–B in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 5. A–B, Boettcheria latisterna: A, distiphallus, lateral; B, styli, anterior (arrow = anterior juxtal process of Roback, 1954). C–F, Dexosarcophaga transita: C, styli, anterior; D, distiphallus, lateral; E, styli, lateral; F, median stylus, anterior. Abbreviations: J, juxta; LS, lateral stylus; MS, median stylus; PT, phallic tube; V, vesica.
Figure 4. A–D in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 4. A–D, Blaesoxipha (Gigantotheca) plinthopyga: A, distiphallus, lateral; B, distiphallus, anterior; C, dissected phallus, anterodorsal; D, median stylus and sperm duct, posteroventral. E–F, Blaesoxipha (s.s.) setosa: E, distiphallus, lateral; F, distiphallus, anterior. G–I, Blaesoxipha (Kellymyia) kellyi: G, distiphallus, lateral; H, distiphallus, anterior; I, median stylus. Abbreviations: EA, ejaculatory apodeme; J, juxta; MS, median stylus; PT, phallic tube; SD, sperm duct.
Figure 1 in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 1. Sarcophaga (Neosarcophaga) occidentalis: A, male postabdomen, left lateral; B, sternite 5, ventral; C, bacilliform sclerites, anterolateral; D, epandrium, cerci and surstyli, posterior.
Figure 2 in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 2. Sarcophaga (Neosarcophaga) occidentalis: A, phallus, left lateral; B, distiphallus, anterior, left harpes removed; C, distiphallus, posterior.
Figure 3. A in Towards a phylogeny of the flesh flies (Diptera: Sarcophagidae): morphology and phylogenetic implications of the acrophallus in the subfamily Sarcophaginae
Figure 3. A, Sarcophaga (s.s.) carnaria. B, Sarcophaga (Neobellieria) triplasia. Syntergosternite 7 + 8, vestige of tergite 6, sternites 5 and 6, dorsal.
Text-fig. 16. Length-width scatter diagram of isolated molars of Sayimys hintoni n. sp. and S. cf. minor from sites H.-SGP 81.14a (lower Manchar Formation, Sind, Pakistan) with the size-cloud outlines of molars of the large sample of S. chinjiensis from H.-GSP.24 shown in Text-fig. 17. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 16. Length-width scatter diagram of isolated molars of Sayimys hintoni n. sp. and S. cf. minor from sites H.-SGP 81.14a (lower Manchar Formation, Sind, Pakistan) with the size-cloud outlines of molars of the large sample of S. chinjiensis from H.-GSP.24 shown in Text-fig. 17.
Text-fig. 15. Lightly worn molars of Sayimys hintoni n. sp. (f, g, h) and S. cf. minor (e and i) from locality H.-GSP81.14a and S. chinjiensis from H.-GSP82.24 (a, b, c, d). Upper molars: occlusal surfaces and labial sides, lower molars occlusal surfaces and lingual sides. Side views horizontally-mirrored, anterior indicated by arrows. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 15. Lightly worn molars of Sayimys hintoni n. sp. (f, g, h) and S. cf. minor (e and i) from locality H.-GSP81.14a and S. chinjiensis from H.-GSP82.24 (a, b, c, d). Upper molars: occlusal surfaces and labial sides, lower molars occlusal surfaces and lingual sides. Side views horizontally-mirrored, anterior indicated by arrows.
Text-fig. 8. Wear stages and height (h) of cheek teeth of Sayimys giganteus from Keseköy. Height in mm of the entoconid (arrow) in lower cheek teeth and paracone (arrow) in upper cheek teeth. Shown are the high value and a low value for each wear stage. Note that h of the different wear stages may show large overlaps, in particular in those of worn teeth. This is due to the often-irregular occlusal surfaces of older individuals. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 8. Wear stages and height (h) of cheek teeth of Sayimys giganteus from Keseköy. Height in mm of the entoconid (arrow) in lower cheek teeth and paracone (arrow) in upper cheek teeth. Shown are the high value and a low value for each wear stage. Note that h of the different wear stages may show large overlaps, in particular in those of worn teeth. This is due to the often-irregular occlusal surfaces of older individuals.
Text-fig. 11. Cheek teeth of Sayimys giganteus from Keseköy. Anterior sides are indicated by arrows. Top row: labial sides of M3, M2, M1 and DP4, images horizontally-mirrored. Second row: occlusal surfaces of M3, M2, M1 and DP4 of the same specimens. Third row: lingual sides of m3, m2, m1 and dp4, images horizontally-mirrored. Lower row: occlusal surfaces of m3, m2, m1 and dp4 of the same specimens. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 11. Cheek teeth of Sayimys giganteus from Keseköy. Anterior sides are indicated by arrows. Top row: labial sides of M3, M2, M1 and DP4, images horizontally-mirrored. Second row: occlusal surfaces of M3, M2, M1 and DP4 of the same specimens. Third row: lingual sides of m3, m2, m1 and dp4, images horizontally-mirrored. Lower row: occlusal surfaces of m3, m2, m1 and dp4 of the same specimens.
Text-fig. 13. Ranges of the length of the m3 based on data from the literature, see Text-fig. 12 for explanation. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 13. Ranges of the length of the m3 based on data from the literature, see Text-fig. 12 for explanation.
Text-fig. 10. Upper cheek teeth of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 10. Upper cheek teeth of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers.
Text-fig. 12. Ranges of the length of the dp4 based on data from the literature. Vertical scale in Ma, the samples are from the Siwaliks (black) and Turkey, Greece and Arabia (red). Type localities of species are indicated with an asterisk. The Y and Z sites are from Baskin (1996), its size ranges are composed of data from several localities and the vertical arrowed broken line indicates the age range of these sites. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 12. Ranges of the length of the dp4 based on data from the literature. Vertical scale in Ma, the samples are from the Siwaliks (black) and Turkey, Greece and Arabia (red). Type localities of species are indicated with an asterisk. The Y and Z sites are from Baskin (1996), its size ranges are composed of data from several localities and the vertical arrowed broken line indicates the age range of these sites.
Text-fig. 6. Histograms of the length of Sayimys giganteus m1–m2 and M1–M2 from Keseköy showing bimodality. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 6. Histograms of the length of Sayimys giganteus m1–m2 and M1–M2 from Keseköy showing bimodality.
Text-fig. 9. Lower molars and premolars of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 9. Lower molars and premolars of Sayimys giganteus from Keseköy and Yapıntı (= YAP numbers) shown as right specimens. Left side specimens are shown in mirror image, these have underlined specimen numbers.
Text-fig. 7. Scatter diagram of molar length against the ratio anterior width / posterior width of upper molars of S. giganteus from Keseköy. in An Exceptional Large Sample Of The Early Miocene Ctenodactyline Rodent Sayimys Giganteus, Specific Variation And Taxonomic Implications
Text-fig. 7. Scatter diagram of molar length against the ratio anterior width / posterior width of upper molars of S. giganteus from Keseköy.
Structural implications of traditional agricultural landscapes on the functional diversity of birds near the Korean Demilitarized Zone
<p><span>Bird assemblages are sensitive to changes in landscape composition and the environment, such as those that result from drought. In this study, the relationship between landscape composition and avian functional diversity in traditional agricultural ecosystems in the Civilian Control Zone (CCZ) of Korea was examined. In addition, the resilience of biodiversity to changes in landscape elements resulting from drought conditions was investigated. The traditional agricultural landscape (TAL) of the sites studied was divided into three types: TAL 1 had a high proportion of rice paddies, TAL 2 included large forest areas, and TAL 3 represented areas with drylands. Of these, TAL 1 showed the highest species richness and functional richness, but these measures were most vulnerable to drought. Meanwhile, TAL 2 showed that the bird communities were more tolerant under drought event. This study shows that to conserve and enhance the diversity of birds in traditional agricultural landscapes of Northeast Asia, active management of forest areas is needed to protect bird populations. In addition, commercial pressures to develop this area will require urgent biodiversity conservation plans to protect the unique biodiversity of the Korean CCZ. This study thus provides landscape management guidance for conservation planning.Bird assemblages are sensitive to changes in landscape composition and the environment, such as those that result from drought. In this study, the relationship between landscape composition and avian functional diversity in traditional agricultural ecosystems in the Civilian Control Zone (CCZ) of Korea was examined. In addition, the resilience of biodiversity to changes in landscape elements resulting from drought conditions was investigated. The traditional agricultural landscape (TAL) of the sites studied was divided into three types: TAL 1 had a high proportion of rice paddies, TAL 2 included large forest areas, and TAL 3 represented areas with drylands. Of these, TAL 1 showed the highest species richness and functional richness, but these measures were most vulnerable to drought. </span>Meanwhile, TAL 2 showed that the bird communities were more tolerant under drought event. <span>This study shows that to conserve and enhance the diversity of birds in traditional agricultural landscapes of Northeast Asia, active management of forest areas is needed to protect bird populations. In addition, commercial pressures to develop this area will require urgent biodiversity conservation plans to protect the unique biodiversity of the Korean CCZ. This study thus provides landscape management guidance for conservation planning.</span></p>
Dataset of Waves generated by discrete and sustained gas eruptions with implications for submarine volcanic tsunamis
<p>This dataset contains all the data used to plot figures in the manuscript "Waves generated by discrete and sustained gas eruptions with implications for submarine volcanic tsunamis" by Yaxiong Shen, Colin Whittaker, Emily Lane, James White, William Power and Bruce Melville submitted to Geophysical Research Letters.</p> <p>The folder "jetplumefountainquantification" contains data for figure 1.</p> <p>The wavedata.xlsx contains wave data and plume rise velocity data. </p> <p>The MATLAB script fig1.m is used to visualise the jet-plume-fountain evolution.</p>
Supplementary material 4 from: Colgan DJ, Ahyong ST, Mardon K, Brereton IM (2021) Rare specimen identification in an un-integrated taxonomy: implications of DNA sequences from a Taiwanese Philine (Mollusca, Philinidae). ZooKeys 1060: 93-110. https://doi.org/10.3897/zookeys.1060.28809
Figure S3. Phylogenetic relationships of C.559479 based on Maximum Likelihood analysis of the histone H3 dataset.
Supplementary material 3 from: Colgan DJ, Ahyong ST, Mardon K, Brereton IM (2021) Rare specimen identification in an un-integrated taxonomy: implications of DNA sequences from a Taiwanese Philine (Mollusca, Philinidae). ZooKeys 1060: 93-110. https://doi.org/10.3897/zookeys.1060.28809
Figure S2. Phylogenetic relationships of C.559479 based on maximum likelihood analysis of the D1 28S rRNA dataset
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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.