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zenodo32/100

FIGURE 2. Wing, dorsal view. A in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 2. Wing, dorsal view. A. Manota yongi sp. n. (holotype). B. Manota oligochaeta sp. n. (paratype). Scale 0.50 mm.

opennotspecifiedMar 2006View details →
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FIGURE 5. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 5. Antennal flagellomere 4, lateral view (A, D); hypopygium, ventral (B, E) and dorsal view (C, F). A, B, C. Manota ovata sp. n. (A, C paratype; B holotype). D, E, F. Manota angustata sp. n. (D, E holotype; F paratype). Scale for A and D 0.05; for B, C, E, and F 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 11. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 11. Antennal flagellomere 4 (A) and flagellomeres 3, 4, and 5 (D), lateral view; and hypopygium in ventral (B, E) and in dorsal (C, F) view. A, B, C. Manota pectinata sp. n. (A, B holotype; C paratype). D, E, F. Manota acutangula sp. n. (D, E holotype; F paratype). Scale for A and D 0.05 mm; for B, C, E, and F 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 16. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 16. Antennal flagellomere 4, lateral view (A, C); hypopygium, ventral (B, D) and dorsal view (E). A, B. Manota perpusilla sp. n. (holotype). C, D, E. Manota oligochaeta sp. n. (C, D holotype; E paratype). Scale for A and C 0.05 mm; for B, D, and E 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 4. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 4. Antennal flagellomere 4, lateral view (A, C) and hypopygium, ventral view (C, D). A, B. Manota yongi sp. n. (holotype). C, D. Manota pollex sp. n. (holotype). Scale for A and C 0.05 mm, for B and D 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 15. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 15. Antennal flagellomere 4, lateral view (A, D); hypopygium, ventral (B, E) and dorsal view (C, F). A, B, C. Manota horrida sp. n. (A, B holotype; C paratype). D, E, F. Manota duplex sp. n. (D, F paratype; E holotype). Scale for A and D 0.05 mm; for B, C, E, and F 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 7. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 7. Antennal flagellomere 4, lateral view (A, D); hypopygium, dorsal view (B); cercus and apicomesial part of gonocoxa, dorsal view (C); and hypopygium, ventral view (E). A, B, C. Manota simplex sp. n. (holotype). D, E. Manota ulu sp. n. (holotype). Scale for A and D 0.05 mm; for B, C, and E 0.10 mm.

opennotspecifiedMar 2006View details →
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FIGURE 14. Antennal flagellomere 4 in Diversity of Manota Williston (Diptera: Mycetophilidae) in a Malaysian rainforest: description of twenty-seven new sympatric species

FIGURE 14. Antennal flagellomere 4, lateral view (A, D); hypopygium, ventral (B, E) and dorsal view (C, F). A, B, C. Manota cerciflex sp. n. (A, B holotype; C paratype). D, E, F. Manota pappi sp. n. (A, C paratype; B holotype). Scale for A and D 0.05 mm; for B, C, E, and F 0.10 mm.

opennotspecifiedMar 2006View details →
zenodo32/100

FIGURES 11, 12 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURES 11, 12. Aleiodes quasiburrus (male) NEW SPECIES. Figure 11. Habitus. Figure 12. Fourth metasomal tergite (arrow). Note that it is only slightly larger than succeeding tergite, shiny and unsculptured except for setal pits, unlike Aleiodes coxalis (Spinola) species-group species.

opennotspecifiedJul 2021View details →
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FIGURE 1 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURE 1. Faces of Braconidae. a: Normal condition. Clypeus extending to mandibles or partly over them. b: Cyclostome condition present in Aleiodes. Clypeus is arched over concave labrum forming a mouth-like structure.

opennotspecifiedJul 2021View details →
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FIGURES 4, 5 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURES 4, 5. Characteristics of Aleiodes. Figure 4. Mummy of Aleiodes (Tetrasphaeropyx) reisi Fortier host (Fortier, 2009). The host mummy of Aleiodes is the hardened, thickened skin of the last larval host instar. When the Aleiodes larva completes its larval development inside the body of the lepidopteran larval host, it kills the host and pupates inside the mummy. The arrow indicates the exit hole cut by the emergent adult wasp. Figure 5. Aleiodes wings (Fortier, 2009), showing abbreviations for names of veins. Cells are regions bordered by veins. The marginal cell of the hind wing is labeled with the full name.

opennotspecifiedJul 2021View details →
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FIGURES 2 & 3 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURES 2 & 3. Characteristics of genus Aleiodes. Figure 2. First and second metasomal tergites of A. okanoganensis. a. basal triangle. b. median carina. Note the costate carinae on the second metasomal tergite. MT I: first metasomal tergite; MT II: second metasomal tergite. Figure 3. Female genitalia of Aleiodes okanoganensis. a. ovipositor. b. ovipositor sheath. Compared to many other parasitoid wasps, these structures are short in Aleiodes, adapted for attacking surface feeding Lepidoptera larvae.

opennotspecifiedJul 2021View details →
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FIGURES 9, 10 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURES 9, 10. Aleiodes okanoganensis (female) NEW SPECIES. Figure 9. Habitus. Note dark pigmentation on propodeum and venter of mesothorax. Figure 10. Fourth metasomal tergite. Note that it is sculptured and much larger than succeeding tergites. These character states together are unique to species in the Aleiodes coxalis (Spinola) species-group. Punctations in apical half are setal pits.

opennotspecifiedJul 2021View details →
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FIGURES 6–8 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURES 6–8. Aleiodes khalafi (female) NEW SPECIES. Figure 6. Habitus. Figure 7. Dorsal view showing sculpturing of propodeum (pr) and metasomal tergites. Figure 8. Closeup of fourth metasomal tergite (arrow). Note that fourth metasomal tergite is sculptured and is much larger than succeeding posterior tergites. These character states together are unique to species in the Aleiodes coxalis (Spinola) species-group.

opennotspecifiedJul 2021View details →
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FIGURE 13 in Aleiodes (Hymenoptera, Braconidae, Rogadinae) diversity in Washington U.S.A including three new species

FIGURE 13. Variation in shapes of hind wing vein RS in Aleiodes species. a. Vein RS sinuate, arching anteriorly at middle (arrow). Marginal cell narrowest in middle. This character state is found in Aleiodes coxalis (Spinola) species group species, but not found in Aleiodes gasterator (Jurine) species-group species. b. Vein RS either straight or angling posteriorly in apical half; not sinuate. Marginal cell not narrowest in middle. This character state is found in Aleiodes gasterator (Jurine) species-group species, such as Aleiodes quasiburrus NEW SPECIES, but not in Aleiodes coxalis (Spinola) species-group species such as Aleiodes khalafi NEW SPECIES and Aleiodes okanoganensis NEW SPECIES.

opennotspecifiedJul 2021View details →
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FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com] in Contributions of biogeographical functions to species accumulation may change over time in refugial regions

FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com]

opennotspecifiedMay 2019View details →
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FIGURE 2 Pentatrocha gigantea n. gen., n in Diversity of cryptic Metazoa in Australian freshwaters: a new genus and two new species of sessile rotifer (Rotifera, Monogononta, Gnesiotrocha, Flosculariidae)

FIGURE 2 Pentatrocha gigantea n. gen., n. sp., trophi SEM pictures. 2a: frontal, detail; 2b: frontal, 2c: caudal view. Scale bars: 10 µm.

opennotspecifiedApr 2008View details →
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FIGURE 6.Floscularia wallacei n in Diversity of cryptic Metazoa in Australian freshwaters: a new genus and two new species of sessile rotifer (Rotifera, Monogononta, Gnesiotrocha, Flosculariidae)

FIGURE 6.Floscularia wallacei n. sp., trophi SEM pictures. 6a: frontal view, 6b: caudal view, 6c: detail. Scale bars: 10 µm.

opennotspecifiedApr 2008View details →
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FIGURE 5. Floscularia wallacei n in Diversity of cryptic Metazoa in Australian freshwaters: a new genus and two new species of sessile rotifer (Rotifera, Monogononta, Gnesiotrocha, Flosculariidae)

FIGURE 5. Floscularia wallacei n. sp., neck spines, SEM pictures. 5a: dorsal, 5b: lateral. Scale bar10 µm.

opennotspecifiedApr 2008View details →
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FIGURE 3. Octotrocha speciosa Thorpe, trophi SEM pictures. 3a in Diversity of cryptic Metazoa in Australian freshwaters: a new genus and two new species of sessile rotifer (Rotifera, Monogononta, Gnesiotrocha, Flosculariidae)

FIGURE 3. Octotrocha speciosa Thorpe, trophi SEM pictures. 3a: caudal; 3b: frontal, 3c: frontal, detail with left ramus, uncus and manubrium view. Scale bars: 10 µm.

opennotspecifiedApr 2008View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record