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Figure 10 from: van Noort S, Lahey Z, Talamas EJ, Austin AD, Masner L, Polaszek A, Johnson NF (2021) Review of Afrotropical sceliotracheline parasitoid wasps (Hymenoptera, Platygastridae). In: Lahey Z, Talamas E (Eds) Advances in the Systematics of Platygastroidea III. Journal of Hymenoptera Research 87: 115-222. https://doi.org/10.3897/jhr.87.73770
Figure 10 Allotropa species female (SAMC) (SAM-HYM-P034571) A habitus, lateral view B habitus, dorsal view C head, mesosoma, dorsal view D propodeum, metasoma, dorsal view E head, anterior view (inset: data labels) F wings, ventral view.
Figure 40 from: van Noort S, Lahey Z, Talamas EJ, Austin AD, Masner L, Polaszek A, Johnson NF (2021) Review of Afrotropical sceliotracheline parasitoid wasps (Hymenoptera, Platygastridae). In: Lahey Z, Talamas E (Eds) Advances in the Systematics of Platygastroidea III. Journal of Hymenoptera Research 87: 115-222. https://doi.org/10.3897/jhr.87.73770
Figure 40 Sceliotrachelus karooensis van Noort, sp. nov. male paratype (SAMC) (SAM-HYM-P049534) A head, mesosoma, dorsal view B head, mesosoma, lateral view C mesoscutum, propodeum, T1,2, dorsal view D metasoma, hind leg, lateral view E propodeum, metasoma dorsal view F fore wing (inset: data labels).
Figure 3 from: Heneberg P, Bogusch P, Astapenková A (2024) Rearing Thyridanthrax fenestratus (Diptera, Bombyliidae) on Pemphredon fabricii (Hymenoptera, Crabronidae) prepupae. Journal of Hymenoptera Research 97: 1-13. https://doi.org/10.3897/jhr.97.110282
Figure 3 Representative figure of the 96-well plate at D10 with typically developing P. fabricii (already pupated, two to four days ahead of the metamorphosis to the adults) treated with penconazole (50 μg mL−1) and with prepupae in wells D7, D8, and G5, which are parasitized by Th. fenestratus. The parasitized prepupae did not pupate and remained paralyzed and were killed within the ensuing four days.
Figure 4 from: Heneberg P, Bogusch P, Astapenková A (2024) Rearing Thyridanthrax fenestratus (Diptera, Bombyliidae) on Pemphredon fabricii (Hymenoptera, Crabronidae) prepupae. Journal of Hymenoptera Research 97: 1-13. https://doi.org/10.3897/jhr.97.110282
Figure 4 Representative figures illustrating critical events in the development of Th. fenestratus on overwintering prepupae of P. fabricii. In bombyliid flies, the first stage, triungulin, is active and immediately molts after attaching to its host to the second stage (likely D6), which has already attached itself and is not distinctly curved. This stage can overwinter (as does the pupa). Early third instar (likely D8) and late third instar (likely D14) can be diagnosed by their characteristic curvature. D24 and D34 represent pupae.
Figure 1 from: Heneberg P, Bogusch P, Astapenková A (2024) Rearing Thyridanthrax fenestratus (Diptera, Bombyliidae) on Pemphredon fabricii (Hymenoptera, Crabronidae) prepupae. Journal of Hymenoptera Research 97: 1-13. https://doi.org/10.3897/jhr.97.110282
Figure 1 Map of examined sampling sites that were positive for P. fabricii (circles). Empty circles indicate sampling sites where only P. fabricii was found. Green circles indicate sites where P. fabricii was parasitized by Th. fenestratus. Source data are available in Suppl. material 1.
Figure 2 from: Heneberg P, Bogusch P, Astapenková A (2024) Rearing Thyridanthrax fenestratus (Diptera, Bombyliidae) on Pemphredon fabricii (Hymenoptera, Crabronidae) prepupae. Journal of Hymenoptera Research 97: 1-13. https://doi.org/10.3897/jhr.97.110282
Figure 2 Time-lapse evidence of the development of Th. fenestratus under laboratory conditions following cold-induced diapause. The X-axis indicates days elapsed since the termination of cold-induced diapause. Individual lines represent photographs of the same individual. The individual in the second line spent the cold-induced diapause as a fully grown larva; all others spent the winter attached to the defecated prepupa but did not grow before the cold-induced diapause. Letters indicate the treatment (DMSO = control, P = penconazole, D = difeconazole, T = tebuconazole; numbers (200, 400, 500, 800, 1200, 2000) indicate the dilution of the study compounds (for more details, refer to Heneberg and Bogusch 2022); letters with numbers indicate the positions in 96-well plates.
Supplementary material 1 from: Heneberg P, Bogusch P, Astapenková A (2024) Rearing Thyridanthrax fenestratus (Diptera, Bombyliidae) on Pemphredon fabricii (Hymenoptera, Crabronidae) prepupae. Journal of Hymenoptera Research 97: 1-13. https://doi.org/10.3897/jhr.97.110282
Coordinates of sampling sites used to generate Fig. 1
Fig 9 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 9 Frequencies of Patanga japonica last instar nymphs that hatched on June 14, July 21, and August 12 and reared in a group in outdoor cages. For black patterning grades, see Fig. 1.
Fig 8 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 8 Effects of visual stimuli from five nymphs on the induction of black patterns in isolated-reared nymphs of Patanga japonica. A. Experimental setup; B. Frequencies of last instar test nymphs in different black patterning grades; C. Body colors in the three grades observed. For black patterning grades, see Fig. 1.
Fig 7 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 7 Solitary-reared (A, grade 1), group-reared (B, grade 5), and CRZ-injected (C, grade 5) last instar nymphs of Patanga japonica at 30°C and individual reared in a group at 34°C (D, grade 2). The individual in C was reared in isolation and green when injected with 1 nmol CRZ at the fourth stadium. For black patterning grades, see Fig. 1.
Fig 6 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 6 Effects of crowding on the frequencies of Patanga japonica last instar nymphs in different black patterning grades in black, yellow-green (Y-green), and white containers. Five nymphs were reared in each container from May 31 to August 15 at room temperature (25.1°C on average). For black patterning grades, see Fig. 1.
Fig 5 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 5 Body color of Patanga japonica nymphs reared in a group at room temperature. Black patterns appeared at the second stadium onward. The penultimate and last nymphal instars were identified based on wing pad size.
Fig 4 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 4 Effects of substrate color on the frequencies of Patanga japonica last instar nymphs with different background body colors (A), with reddish legs (B), and in different black patterning grades (C). Nymphs were reared individually in black, yellow-green (Y-green) and white containers from May 31 to August 15 at room temperature (25.1°C on average). Different letters in B indicate significant differences in proportions by a χ2 test at 5%. For body colors and black patterning grades, see Fig. 1.
Fig 2 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 2 Variation in body color of Patanga japonica last instar nymphs. Photographs were taken on September 1 (A), October 11 (B), October 21 (C), November 11 (D), September 29 (E), and September 27, 2021 (F).
Fig 3 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 3 Proportions of green and non-green Patanga japonica last instar nymphs observed at a study site in Tsukuba in 2021.
Fig 14 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 14 Body color of Patanga japonica adults. A–D. Variation in body color in field-collected adults; E. Adult reared at 34°C; F. Adults on leaf litter (yellow arrows); G. Non-pigmented and reddish hindwings observed in adults before (left) and after overwintering (right). Black male adult in D was collected on July 7, 2021. Scales are adjusted to make body sizes approximately equal except for F.
Fig 13 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 13 Examples of exuviae shed by Patanga japonica last instar nymphs after various treatments. Exuviae had no color with only a thin black line on the hind femurs in singly reared green nymphs (A), black patterns with a yellow background color in crowd-reared nymphs kept at room temperature (B), and in corazonin-injected nymphs kept at a high temperature (C), and had a few black areas with a bright yellow background color in the thoracic area in nymphs reared at a high temperature (D).
Fig 11 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 11 Body color of Patanga japonica adults that were injected with oil alone (left) or 1 nmol CRZ (right) at the fourth stadium and a darkened uninjected old female observed on June 18 in an outdoor cage (bottom).
Fig 12 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 12 Effect of high temperature on black patterning in Patanga japonica. Frequencies of last instar nymphs in different grades after transfer from outdoor conditions to 34°C and LD 12:12h at the third stadium (September 28, 2022) or kept outdoors continuously as a control (A). Examples showing body color variation at the last nymphal instar under outdoor conditions (B–E) and at 34°C (F–H). Last instar nymph that was injected with CRZ at the fourth stadium and then singly kept at 34°C (I). Black patterning grades are based on Fig. 1.
Fig 1 from: Tanaka S, Kayukawa T (2024) Environmental and hormonal control of body-color polyphenism in Patanga japonica (Orthoptera, Acrididae): Effects of substrate color, crowding, temperature and [His7]-corazonin injection. Journal of Orthoptera Research 33(1): 1-12. https://doi.org/10.3897/jor.33.98133
Fig 1 Examples of the different body colors of the last instar nymphs of Patanga japonica observed during experiments. A. Variation in background color; B. Black patterning grades; C. Nymphs with green and reddish legs. In B, grade 1, no black patterns and only brownish spots or patterns on the abdomen; grade 2, black patterns on the abdomen and some or no brown spots on the thorax; grade 3, distinct black patterns both on the thorax and abdomen but the lateral sides of pronotum without black spots; grade 4, as in grade 3 but the lateral sides of pronotum with distinct black spots; grade 5, as in grade 4 but the lateral sides of pronotum with black markings.
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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.