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Figs. 89–91 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 89–91. SEM micrographs of the postdefecating larva of Megachile minutissima. 89. Head, lateral view, showing slopping profile of cranium. 90. Salivary lips, frontal view. 91. Close-up of upper lip identified by rectangle in fig. 90.
Figs. 80–82 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 80–82. SEM micrographs of the postdefecating larva of Coelioxys decipiens. 80. Antennal papilla, lateral view. 81. Salivary lips, frontal view. 82. Close-up of inner surface of upper lip identified by rectangle in fig. 81.
Figure 20 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figure 20 is a close-up in ventral view of the anterior end of the first instar of Radoszkowskiana rufiventris from which the piece of chorion had been torn away when host and parasite were separate. The peculiar stratum with a papillate outer surface covering the front of the labrum cannot be explained at this time and warrants further investigation to reveal its anatomy and function. Of special interest are the mandibles. Although, as stated above, we thought at first that each had a simple, curved, sclerotized apex, we discov-
Figs. 47, 48 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 47, 48. Photographs of heads of postdefecating larvae, lateral view. 47. Coelioxys decipiens, with hypostomal tubercle and ridge delineated by dashed line. 48. Coelioxys coturnix, with hypostomal ridge delineated by dashed line.
Figs. 14–17 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 14–17. SEM micrographs of midbody segments of first instars of Megachile nigripes and Radoszkowskiana rufiventris, showing differences in spicules, anterior ends toward left, lateral view; for explanation, see text. 14. Two midbody segments of M. nigripes showing sharp-pointed, thornlike spi-
Fig. 18 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Fig. 18. SEM micrographs of egg of Megachile nigripes from which first instar of Radoszkowskiana rufiventris had been removed, leaving behind piece of chorion that had covered its mouthparts, identified by rectangle. Fig. 19. Close-up of piece of chorion of R. rufiventris identified by rectangle in fig. 18.
Fig. 12 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Fig. 12. Photograph of live egg of Radoszkowskiana rufiventris on top of egg of Megachile nigripes, collected on June 1, 2005, dorsal view. Fig. 13. Photograph of same individual of R. rufiventris preserved as pharate first instar with host egg on June 2, 2005, lateral view.
Figs. 3–5 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 3–5. Diagrams of cells and cocoon of Megachile nigripes, lateral views. 3. Taller cell, showing provisions with egg of Radoszkowskiana rufiventris deposited on floating egg of host. 4. Shorter cell with cocoon of M. nigripes. 5. Close-up of cross section of upper end of cocoon of M. nigripes; for explanations, see text.
Fig. 11 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Fig. 11. Diagram of egg Radoszkowskiana rufiventris position on egg of Megachile nigripes found on May 17, 2004, anterior ends to left, dorsal view.
Figs. 6–10 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 6–10. Right mandibles of larval instars of Radoszkowskiana rufiventris, outer views, with apices drawn in maximum profile. 6. First instar, above, outer view with second tooth eclipsed by apical tooth, and, below, ventral view showing basal tooth.7. Second instar. 8. Third instar. 9. Fourth instar. 10. Fifth instar. All figures drawn to same scale.
Figs. 1, 2 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 1, 2. Nesting sites of Megachile nigripes and it cleptoparasites in Tel El Kebir, Egypt. 1. Abundant adults of this solitary bee and its cleptoparasites (as well as of other bees) nesting in adobe wall to the left. 2. Kariman Mahmoud (left) and Soliman M. Kamel standing in front of adobe building showing damage caused by numerous generations of Megachile nigripes and other solitary bees nesting in the walls; large holes left of each of person resulted from our excavations of the nests.
Figs. 23–26 in Investigations on the Biologies and Immature Stages of the Cleptoparasitic Bee Genera Radoszkowskiana and Coelioxys and Their Megachile Hosts (Hymenoptera: Apoidea: Megachilidae: Megachilini)
Figs. 23–26. Photographs of feeding larval instars of Radoszkowskiana rufiventris. 23. First instar three days after collection as egg, on partly consumed host egg. 24. Second instar of same individual with opaque, yellowish abdomen, two days later, and chorion of completely consumed host egg. 25. Probably third instar, different individual; note shiny chorion of host egg to the left of its forebody. 26. Fourth instar of same individual as in figs. 23, 24, nine days after being collected as egg; two days later, larvae became fifth instar.
Figure 1-9 in Distribution and biology of the rare scarab beetle Megatharsis buckleyi Waterhouse, 1891 (Coleoptera: Scarabaeinae: Phanaeini)
Figure 1-9. Megatharsis buckleyi. Unless noted, scale in millimetres. 1-4) Holotype female in the BMNH. Photographs by Harry Taylor (The Natural History Museum photographic unit). 1) Dorsal view. 2) Oblique view. 3) Lateral view. 4) Close-up of head and pronotum. 5) Female collected in Macas, Morona-Santiago, Ecuador (BMNH). Photograph by Harry Taylor. 6) Specimen collected in Macas, Ecuador (MECN). Photograph by Santiago Villamarin. 7-8) Specimen collected in Peru: Depto. Madre de Díos, Río Madre de Díos, CICRA Biological Station, Río Los Amigos. T. Larsen (NMNH). Length 13.1mm. Photographs by Trond Larsen. 7) Dorsal view. 8) Oblique close-up of head and pronotum. 9) Specimen collected in 'Abuna', Rondônia, Brazil (BMNH). Photograph by Harry Taylor.
Figure 10 in Distribution and biology of the rare scarab beetle Megatharsis buckleyi Waterhouse, 1891 (Coleoptera: Scarabaeinae: Phanaeini)
Figure 10. Distribution map for Megatharsis buckleyi Waterhouse. All known confirmed localities are indicated by black circles. The unconfirmed locality of Iquitos is marked by a question mark and the Andean localities presented by Blut (1939) around the city of Cuenca, are shown by a cross.
Figure 1 Aceria alhagi n in A new Aceria species (Acari:Trombidiformes: Eriophyoidea) from West Asia, a potential biological control agent for the invasive weed camelthorn, Alhagi maurorum Medik. (Leguminosae)
Figure 1 Aceria alhagi n.sp.: AD – Antero-dorsal mite; AL – Antero-lateral view of mite; CG – Coxigenital region of female; em – Empodium; GM – Genital region of male; IG – Internal female genitalia; L1 – Leg I of female; LO – Lateral opisthosoma; PM – Postero-lateral mite. Scale bar: 20μm for AD, AL,CG, GM, IG, LO, PM; 10μm for L1; 5μm for em.
Figure 2 SEM images ofAceria alhagi n in A new Aceria species (Acari:Trombidiformes: Eriophyoidea) from West Asia, a potential biological control agent for the invasive weed camelthorn, Alhagi maurorum Medik. (Leguminosae)
Figure 2 SEM images ofAceria alhagi n. sp.: A – prodorsal shield; B – tarsal empodia on legs I and II; C – ventral view of coxigenital area of female; D – ventral view of coxigenital area of male.
Figure 1 in Biological effects of three bacterial species on Tetranychus urticae (Acari: Tetranychidae) infesting eggplant under laboratory and greenhouse conditions
Figure 1 Pictures of dead mite individuals after spray with the pathogenic bacteria: A – Acinetobacter sp.; B –B. subtilis and C –B. qassimus
Figures 53–63 in The systematics and biology of the Costa Rican species of parasitic wasps in the Thyreodon genus-group (Hymenoptera: Ichneumonidae)
Figures 53–63. Apex of metasoma and male genital capsule, lateral; 53, T. maculipennis; 54, T. erythrocera; 55, T. whitfieldi; 56, T. laticinctus; 57, T. zitaniae; 58, T. papei; 59, T. morosus; 60, T. schauffi; 61, T. darlingi; 62, T. rufothorax; 63, T. atriventris.
Figures 47–52. 47–50 in The systematics and biology of the Costa Rican species of parasitic wasps in the Thyreodon genus-group (Hymenoptera: Ichneumonidae)
Figures 47–52. 47–50, mesoscutum and pronotum, lateral; 47, T. papei; 48, T. deansi; 49, T. erythrocera; 50, T. sharkeyi. 51–52, apex of metasoma and male genital capsule, lateral; 51. Rhynchophion flammipennis; 52, R. woodi.
Figures 39–46. Thyreodon species. 39–40 in The systematics and biology of the Costa Rican species of parasitic wasps in the Thyreodon genus-group (Hymenoptera: Ichneumonidae)
Figures 39–46. Thyreodon species. 39–40, head, postero-lateral; 39, T. erythrocera; 40, T. sharkeyi. 41–44, head, dorsal; 41, T. rivinae; 42, T. maculipennis; 43, T. atriventris; 44. T. woodleyi. 45–46, mesoscutum and pronotum, lateral; 45, T. walkerae; 46, T. woodleyi.
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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.