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Figs 13–18. Male genitalia. — 13–14. Belbina bergrothi. 13. Lateral view. 14. Dorsal view. — 15–16. B. bloetei. 15. Lateral view. 16. Dorsal view. — 17–18. B in Revision of the Malagasy lanternfly genus Belbina Stål, 1863, with two new species (Hemiptera: Fulgoromorpha: Fulgoridae)
Figs 13–18. Male genitalia. — 13–14. Belbina bergrothi. 13. Lateral view. 14. Dorsal view. — 15–16. B. bloetei. 15. Lateral view. 16. Dorsal view. — 17–18. B. bourgoini sp. nov. 17. Lateral view. 18. Dorsal view. — An = anal tube, Py = pygofer, G = gonostylus. Photographs by Y. Laurent & I. Bachy.
Figs 24–29. Male genitalia. — 24–25. Belbina lambertoni. 24. Lateral view. 25. Dorsal view. — 26– 27. B. madagascariensis. 26. Lateral view. 27. Dorsal view. — 28–29. B. nympha. 28. Lateral view. 29 in Revision of the Malagasy lanternfly genus Belbina Stål, 1863, with two new species (Hemiptera: Fulgoromorpha: Fulgoridae)
Figs 24–29. Male genitalia. — 24–25. Belbina lambertoni. 24. Lateral view. 25. Dorsal view. — 26– 27. B. madagascariensis. 26. Lateral view. 27. Dorsal view. — 28–29. B. nympha. 28. Lateral view. 29. Dorsal view. — An = anal tube, Py = pygofer, G = gonostylus. Photographs by Y. Laurent & I. Bachy.
Fig. 5. Male habitus, lateral view. A in Species of the genus Chrysotus Meigen, 1824 (Diptera: Dolichopodidae) from Japan, with descriptions of two new species
Fig. 5. Male habitus, lateral view. A. Chrysotus masunagai Negrobov, Kumazawa & Tago sp. nov., Ƌ, paratype, coll. 15 May 2010. B. Chrysotus saigusai Negrobov, Kumazawa & Tago sp. nov., Ƌ, paratype, coll. 8 Jul. 2012.
Fig. 5. Leiobunum, male genitalia. A–C. L. rupestre Herbst, 1799 in The Leiobunum rupestre species group: resolving the taxonomy of four widespread European taxa (Opiliones: Sclerosomatidae)
Fig. 5. Leiobunum, male genitalia. A–C. L. rupestre Herbst, 1799, Germany, Baden-Württemberg, CJM1954. A. Ventral view. B. Lateral view. C. Cross-section. — D–F. L. gracile Thorell, 1876, Denmark, 2 km N of Skaerbaek, CJM3530. D. Ventral view. E. Lateral view. F. Cross-section. — G–J. L. apenninicum (Martens, 1969), France, Alpes-Maritimes, CJM1508. G. Ventral view. H. Lateral view. J. Cross-section. Arrows indicate the area of the respective cross-sections.
Figs 41–58. Male elytra. 41 in High diversity and endemism in the genus Cautires Waterhouse, 1879 (Coleoptera: Lycidae) from the Malay mountain forests, with the descriptions of fourteen new species
Figs 41–58. Male elytra. 41. Cautires alexae sp. nov. 42. C. andujari sp. nov. 43. C. arribasae sp. nov. 44. C. berembanensis sp. nov. 45. C. campestris sp. nov. 46. C. communis sp. nov. 47. C. griseus Kleine, 1930. 48. C. jasarensis sp. nov. 49. C. katarinae sp. nov. 50. C. kirstenae sp. nov. 51. C. kotatinggensis sp. nov. 52. C. linardi sp. nov. 53. C. maseki sp. nov. 54. C. pahangensis sp. nov. 55. C. nervosus Kleine, 1926. 56. C. renatae sp. nov. 57. C. reverandi Pic, 1925. 58. C. simillimus Kleine, 1926. Scale bars = 1.0 mm.
Figs 21–38. Male pronotum. 21 in High diversity and endemism in the genus Cautires Waterhouse, 1879 (Coleoptera: Lycidae) from the Malay mountain forests, with the descriptions of fourteen new species
Figs 21–38. Male pronotum. 21. Cautires alexae sp. nov. 22. C. andujari sp. nov. 23. C. arribasae sp. nov. 24. C. berembanensis sp. nov. 25. C. campestris sp. nov. 26. C. communis sp. nov. 27. C. griseus Kleine, 1930. 28. C. jasarensis sp. nov. 29. C. katarinae sp. nov. 30. C. kirstenae sp. nov. 31. C. kotatinggensis sp. nov. 32. C. linardi sp. nov. 33. C. maseki sp. nov. 34. C. pahangensis sp. nov. 35. C. nervosus Kleine, 1926. 36. C. renatae sp. nov. 37. C. reverandi Pic, 1925. 38. C. simillimus Kleine, 1926. — 39–40. Male elytra costae, detail: 39. C. andujari sp. nov. 40. C. campestris sp. nov. Scale bars = 0.5 mm.
Figure 1 in Phytoseiidae of La Réunion Island (Acari: Mesostigmata): three new species and two males described, new synonymies, and new records
Figure 1Male of Neoseiulus houstoni Schicha: a – Dorsal shield and peritreme; b – Ventral shields; c – Spermatodactyl.
Draft genome assembly of a Japanese Oikopleura dioica male individual (O3), using Nanopore long reads.
<p>This draft assembly was used to validate the chrY scaffolds of the OSKA2016 reference genome in the publication “A genome database for a Japanese population of the larvacean Oikopleura dioica”, Development Growth and Differentiation, Wang and coll., 2020 (in press). It is provided as supplemental data for the reproducibility of this work; please note that no further polishing has been done to correct sequencing errors.</p> <p>Genome sequence reads were produced on a MinION sequencer (Oxford Nanopore Technologies) using high-molecular weight DNA from a male individual of the Oikopleura dioica species of zooplankton. The individual was related to the laboratory strain established from a western Japanese population that was used to produce the OSKA2016 reference genome. The raw reads were basecalled with the Guppy software version 3.3.0 using its dna_r9.4.1_450bps algorithm, and deposited in the European Nucleotide Archive (Study ID: PRJEB38559). The draft assembly was made with the Flye software version 2.7 with the options --genome-size 65m and --min-overlap 3000.</p>
Data from: Male and female bees show large differences in floral preference
<p>Intraspecific variation in foraging niche can drive food web dynamics and ecosystem processes. In particular, male and female animals can exhibit different, often cascading, impacts on their interaction partners. Despite this, studies of plant-pollinator interaction networks have focused on the partitioning of the floral community between pollinator species, with little attention paid to intraspecific variation in plant preference between male and female bees. We designed a field study to evaluate the strength and prevalence of sexually dimorphic foraging, and particularly resource preferences, in bees. We observed bees visiting flowers in semi-natural meadows in New Jersey, USA. To detect differences in flower use against a shared background of resource (flower) availability, we maximized the number of interactions observed within narrow spatio-temporal windows. To distinguish observed differences in bee use of flower species, which can reflect abundance patterns and sampling effects, from underlying differences in bee preferences, we analyzed our data with both a permutation-based null model and random effects models. We found that the diets of male and female bees of the same species were often dissimilar as the diets of different species of bees. Furthermore, we demonstrate differences in preference between male and female bees. We show that intraspecific differences in preference can be robustly identified among hundreds of unique species-species interactions, without precisely quantifying resource availability, and despite high phenological turnover of both bees and plant bloom. Given the large differences in both flower use and preferences between male and female bees, ecological sex differences should be integrated into studies of bee demography, plant pollination, and coevolutionary relationships between flowers and insects.</p>
Male protest stridulatory sounds of Phyllophorina kotoshoensis Shiraki, 1930 (Orthoptera: Tettigonioidea: Phaneropteridae: Phyllophorinae)
<p>The male stridulatory protest sounds of Phyllophorina kotoshoensis Shiraki, 1930 from Taiwan were recorded using a digital bat detector Pettersson D1000X with a sampling rate of 192 kHz. Air temperature at recording: 20 <sup>o</sup>C. Distance between a microphone and the katydid: about 10 cm.</p> <p>Recordist: K.-G. Heller.</p> <p>Katydid used the coxosternal sound apparatus.</p>
Figure 1 in New species of Australopericoma Vaillant (Diptera: Psychodidae) from the Brazilian semiarid region and key to males of the genus
Figure 1. Australopericoma paraibana Cordeiro & Bravo sp. nov. (A) anterior view of head, palpi and antenna; (B) head, posterior view; (C) antenna, apical flagellomeres; (D) flagellomeres showing ascoids; (E) wing; (F) ventral view of male terminalia, showing part of epandrium, cerci, epiproct and hypoproct; (G) dorsal view of male terminalia, showing hypandrium, gonopods and aedeagal complex.
Figure 4. Iporangaia pustulosa male twisting the right tarsus IV in Mode of use of sexually dimorphic glands in a Neotropical harvestman (Arachnida: Opiliones) with paternal care
Figure 4. Iporangaia pustulosa male twisting the right tarsus IV, rubbing it against the substrate (seta).
Figs 40-42. Remotomyia brunales spec. nov. paratype male genitalia. 40. Lateral. 41. Ventral. 42 in The Genus Daspletis Loew, 1858 And The Description Of Two New Genera, Anasillomos And Remotomyia (Diptera: Asilidae: Stenopogoninae)
Figs 40-42. Remotomyia brunales spec. nov. paratype male genitalia. 40. Lateral. 41. Ventral. 42. Dorsal.
Figs 1-5. Anasillomos chrysopos spec. nov. paratype male. 1. Antenna, lateral aspect. 2 in The Genus Daspletis Loew, 1858 And The Description Of Two New Genera, Anasillomos And Remotomyia (Diptera: Asilidae: Stenopogoninae)
Figs 1-5. Anasillomos chrysopos spec. nov. paratype male. 1. Antenna, lateral aspect. 2. Head and part of thorax. 3- 5. Genitalia. 3. Lateral. 4. Ventral. 5. Dorsal.
Figs 22-24. Daspletis stenoura spec. nov. paratype male genitalia. 22. Lateral. 23. Ventral. 2 4 in The Genus Daspletis Loew, 1858 And The Description Of Two New Genera, Anasillomos And Remotomyia (Diptera: Asilidae: Stenopogoninae)
Figs 22-24. Daspletis stenoura spec. nov. paratype male genitalia. 22. Lateral. 23. Ventral. 2 4. Dorsal.
Figs 11 15. Daspletis hirtus Ricardo. 11-12. Kalahari Gemsbok Park male. 11. Head. 12. Antenna, lateral aspect. 13- 15. Sawmills topotype male genitalia. 13. Lateral. 14. Ventral. x4 in The Genus Daspletis Loew, 1858 And The Description Of Two New Genera, Anasillomos And Remotomyia (Diptera: Asilidae: Stenopogoninae)
Figs 11 15. Daspletis hirtus Ricardo. 11-12. Kalahari Gemsbok Park male. 11. Head. 12. Antenna, lateral aspect. 13- 15. Sawmills topotype male genitalia. 13. Lateral. 14. Ventral. x4. Dorsal.
Fig. 2. Male genitalia. A in Revalidation and taxonomic revision of Teloneria Aczél (Diptera, Neriidae), with description of two new species
Fig. 2. Male genitalia. A. Teloneria apicata (Edwards, 1919) comb. nov. B. Teloneria bimaculata (Edwards, 1919) comb. nov. C. Teloneria juceliae Sepúlveda & Souza sp. nov. D. Teloneria ladyae Sepúlveda & Souza sp. nov.
Fig. 15. Male genitalia. A–D in Revision of the lanternfly genus Limois Stål, 1863 (Hemiptera: Fulgoromorpha: Fulgoridae) with description of a new species from China
Fig. 15. Male genitalia. A–D. Limois sordida sp. nov., Shanxi, Ningwu, Mt. Luyashan, Ai-ping Dong leg., NWAFU. A. Left lateral view. B. Gonostylus, left lateral view. C. Aedeagus, dorsal view. D. Aedeagus, ventral view. – E–I. Limois westwoodii (Hope, 1843), Myanmar, Nat Ma Taung, RBINS. E. Left lateral view. F. Gonostylus, ventral view. G. Aedeagus, left lateral view. H. Aedeagus, dorsal view. I. Aedeagus, ventral view. – J–N. Limois emelianovi Oshanin, 1908, Vladivostok, Anufriev leg., RBINS. J. Left lateral view. K. Gonostylus, left lateral view. L. Aedeagus, left lateral view. M. Aedeagus, dorsal view. N. Aedeagus, ventral view.
Fig. 14. Male genitalia. A–D in Revision of the lanternfly genus Limois Stål, 1863 (Hemiptera: Fulgoromorpha: Fulgoridae) with description of a new species from China
Fig. 14. Male genitalia. A–D. Limois chagyabensis Chou & Lu, 1981, NWAFU HO088523. A. Left lateral view. B. Gonostylus, ventral view. C. Aedeagus, dorsal view. D. Aedeagus, ventral view. – E–H. Limois guangxiensis Chou & Wang, 1985, NWAFU HO088509. E. Left lateral view. F. Gonostylus, ventral view. G. Aedeagus, dorsal view. H. Aedeagus, ventral view. – I–L. Limois hunanensis Chou & Wang, 1985, NWAFU HO088511. I. Left lateral view. J. Gonostylus, ventral view. K. Aedeagus, dorsal view. L. Aedeagus, ventral view. – M–Q. Limois kikuchii Kato, 1932, Manchuria, K. Kikuchi leg., RBINS. M. Left lateral view. N. Gonostylus, left lateral view. O. Aedeagus, left lateral view. P. Aedeagus, dorsal view. Q. Aedeagus, ventral view.
Fig. 8. A–E. Adult habitus, lateral view. F. Basicosta. A–D. Female. E–F. Male. A in Review of the Eumerus tricolor species group (Diptera: Syrphidae) in Iran, with description of six new species
Fig. 8. A–E. Adult habitus, lateral view. F. Basicosta. A–D. Female. E–F. Male. A. Eumerus brevipilosus Gilasian & van Steenis sp. nov., paratype (HMIM). B. E. coeruleus (Becker, 1913), Ghoochan, Iran (HMIM). C. E. longitarsis Peck, 1979, Mian Jangal, Iran (JSA). D. E. persarum Stackelberg, 1961, Bazman, Iran (JSA). E. E. tricolor (Fabricius, 1798), Paleochori, Greece (JSA). F. E. tadzhikorum Stackelberg, 1949, Chekab Valley, Iran (JSA). Scale bars = 1.0 mm. Abbreviations: ac = anterodorsal costal setae; pc = posterodorsal costal setae.
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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.