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176 results for “flower fly”
Fig. 23 in Paragus caligneus sp. nov., a new Afrotropical species of flower fly (Diptera: Syrphidae)
Fig. 23. Phylogram of the best tree from a maximum likelihood search of the combined dataset using Garli-part v0.97 (ln L = í8463.463783). Numbers above nodes are maximum likelihood bootstrap support values (>50%).
Fig. 24 in Paragus caligneus sp. nov., a new Afrotropical species of flower fly (Diptera: Syrphidae)
Fig. 24. Majority-rule consensus tree from the Bayesian analysis using MrBayes. The Bayesian posterior probability values (>0.5) are given above the nodes.
Figs 1–9 in Paragus caligneus sp. nov., a new Afrotropical species of flower fly (Diptera: Syrphidae)
Figs 1–9. Paragus caligneus sp. nov. 1–3 – holotype male; 1 – lateral view; 2 – frontal view; 3 – dorsal view. 4–7 – paratype female; 4 – dorsal view; 5 – lateral view; 6 – frontal view; 7 – posterior view. 8 – holotype male, labels. 9 – paratype female, label.
Figs 18–22. 18–20 in Paragus caligneus sp. nov., a new Afrotropical species of flower fly (Diptera: Syrphidae)
Figs 18–22. 18–20 – Paragus caligneus sp. nov., male genitalia. 18 – ventral view; 19 – dorsal view; 20 – lateral view. Fig. 21. Paragus caligneus sp. nov., posterior margin of sternum 4. 22 – Paragus borbonicus Macquart, 1842, surstylus in dorsal view.
Figs 10–17. 10–13 in Paragus caligneus sp. nov., a new Afrotropical species of flower fly (Diptera: Syrphidae)
Figs 10–17. 10–13 – Paragus caligneus sp. nov.; 10 – male head, dorsal view; 11 – female head, dorsal view; 12 – female head, frontal view; 13 – male antenna, lateral view. 14–17 – Paragus borbonicus Macquart, 1842; 14 – male head, dorsal view; 15 – female head, dorsal view; 16 – female head, frontal view; 17 – male antenna, lateral view.
Fig. 42 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Fig. 42. The ecological environment of Biema qilianensis Huo & Liu gen. et sp. nov. collection area in China.
Figs 25–41 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Figs 25–41. Biema qilianensis Huo & Liu gen. et sp. nov. 25. Male, head in lateral view. 26. Female, head in frontal view. 27. Antenna, inside view. 28. Male, head in dorsal view. 29. Female, abdomen in dorsal view. 30. Male, abdomen in dorsal view. 31. Wing. 32. Male, terminalia in lateral view. 33. Male, epandrium and appendages in dorsal view. 34. Male, terminalia in ventral view. 35. Male, hypandrium and appendages in lateral view. 36. Male, epandrium and appendages in lateral view. 37. Male, superior lobe in lateral view. 38. Male, epandrium and appendages in ventral view. 39. Phallus in lateral view. 40. Phallus in dorsal view. 41. Phallus in ventral view.
Figs 5–7 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Figs 5–7. Biema wanglangensis Huo & Zhao gen. et sp. nov., paratype, ♀ (ZFMK-DIP-00097119). 5. Habitus, dorsal view. 6. Habitus, left lateral view. 7. Head, frontal view. Scale bars: 5–6 = 1 mm; 7 = 0.5 mm.
Fig. 24 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Fig. 24. The ecological environment of Biema wanglangensis Huo & Zhao gen. et sp. nov. collection area in China.
Figs 2–4 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Figs 2–4. Biema wanglangensis Huo & Zhao gen. et sp. nov., paratype, ♂ (ZFMK-DIP-00097118). 2. Habitus, dorsal view. 3. Habitus, left lateral view. 4. Head, frontal view. Scale bars: 2–3 = 1 mm; 4 = 0.5 mm.
Fig. 43 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Fig. 43. The phylogenetic tree of the tribes Bacchini Bigot, 1883 and Melanostomini Williston, 1885 based on the COI gene. Statistical support values (posterior probability) of BI methods are shown above each node. Groups resulting from jMOTU, GMYC and ABGD tests are indicated on the right side.
Figs 8−23 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Figs 8−23. Biema wanglangensis Huo & Zhao gen. et sp. nov. 8. Male, head in lateral view. 9. Male, head in dorsal view. 10. Female, head in frontal view. 11. Antenna, inside view. 12. Male, abdomen in dorsal view. 13. Female, abdomen in dorsal view. 14. Wing. 15. Male, terminalia in lateral view. 16. Male, terminalia in ventral view. 17. Male, epandrium and appendages in dorsal view. 18. Male, epandrium and appendages in ventral view. 19. Male, epandrium and appendages in lateral view. 20. Male, hypandrium and appendages in lateral view. 21. Superior lobe in lateral view. 22. Phallus. 23. Distal end of phallus in dorsal view.
Fig. 1 in Biema Huo & Zhao gen. nov., a new flower fly genus (Diptera, Syrphidae) from China
Fig. 1. Known distribution of genus Biema Huo & Zhao gen. nov. in China. Pink dot represents Biema qilianensis Huo & Liu gen. et sp. nov.; black dot represents Biema wanglangensis Huo & Zhao gen. et sp. nov.; pink area represents Sichuan Province, China; grey area represents Qinghai Province, China.
Figs 4–6 in In honor of Brian Stuckenberg: Two new Spheginobaccha species of flower flies (Diptera: Syrphidae) from the Afrotropics
Figs 4–6. Spheginobaccha pamela sp. n. Paratype ♂ (Madagascar): (4) habitus, dorsal view; (5) habitus, lateral view; (6) genitalia, lateral view.
Figs 1–3 in In honor of Brian Stuckenberg: Two new Spheginobaccha species of flower flies (Diptera: Syrphidae) from the Afrotropics
Figs 1–3. Spheginobaccha stuckenbergi sp. n. Holotype ♂ (Madagascar): (1) habitus, dorsal; (2) head, lateral view; (3) male genitalia, lateral view.
Data from: Insect pollinators show constancy for different flower traits between the most‐ and less‐preferred plants: a case study of the long‐proboscid tangle‐veined fly
<p>1. The coevolution of insect pollinators and their host plants is a typical example of natural selection; however, it remains unclear as to how insect pollinators avoid overdependence on one peculiar plant. As most insect pollinators exhibit a diet breadth when showing flower constancy, to determine the difference and similarity of most and less-preferred flowers by insect pollinators may be helpful to understand their trade-off between flower constancy and overdependence.</p> <p>2. We addressed this question in the long-proboscid tangle-veined fly (<i>Nemetrinus spp.</i>). Dietary investigation indicates that the flies show constancy for the morphological characteristic of the <i>Delphinium caeruleum</i>, which is the most preferred plant for this Nemestrinidae fly that has blue, long-tubed flowers.</p> <p>3. In a colour selection experiment, focal individuals showed obvious preference for white, which is the colour of less-preferred flowers by the fly in the natural environment. In a scent selection experiment, focal individuals showed obvious preference for <i>D. caeruleum </i>and <i>Dracocephalum heterophyllum</i>, but avoidance to <i>Dasiphora</i><i> fruticosa</i> and <i>Dasiphora davurica</i>. This indicates that long-proboscid tangle-veined flies can forage on other flowers, even the existing of constancy for <i>D. caeruleum</i>, as long as they do not hate the scent. It seems that long-proboscid tangle-veined flies can maximize foraging efficiency by showing constancy for the morphological characteristic of the most preferred plant and for the scent and colour of less-preferred plants.</p> <p>4. The tradeoff of long-proboscid tangle-veined fly in selection of nectar sources may be an adaptation to the risk of overdependence on one plant in evolution.</p>
Data from: Individual-based networks reveal the importance of bee fly (Bombyliidae) pollination in a diverse co-flowering community
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Data from: Insect pollinators show constancy for different flower traits between the most‐ and less‐preferred plants: a case study of the long‐proboscid tangle‐veined fly
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Temporal variation in floral scent emission of a woody plant and flower visiting behaviour of male and female flies
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FIGURE 41 in Revision of the Psilota Meigen, 1822 flower flies (Diptera: Syrphidae) of Australia
FIGURE 41. Lateral and dorsal male genitalia of A, B) P. azurea sp. nov.; C, D) P. basalis Walker; E, F) P. bicolor sp. nov., and G, H) P. brunnipennis sp. nov.. Scale bar =1 mm.
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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)
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DANDI Archive for NWB datasets
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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.