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Figure 1 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 1 Pseudalomya truncaticornis sp. nov. holotype (NMNS ENT 8836-1) A lateral view of the habitus B dorsal view of the habitus. Photographed by Hsuan-Pu Chen.
Figure 2 from: Chen H-P, Kikuchi N, Shiao S-F (2024) Discovery of a new Pseudalomya Telenga, 1930 (Hymenoptera, Ichneumonidae, Ichneumoninae) species from Taiwan and its implications for the systematic position of this genus. Journal of Hymenoptera Research 97: 277-296. https://doi.org/10.3897/jhr.97.119470
Figure 2 Pseudalomya truncaticornis sp. nov. holotype (NMNS ENT 8836-1) A dorsal view of the head B anterior view of the head C lateral view of the head D foreleg E dorsal view of the mesoscutum F dorsal view of the propodeum G dorsal view of the metasomal tergites. Photographed by Hsuan-Pu Chen.
Fig 8 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 8 Correlations of head widths between field-collected females and group-reared G1 (A, B) or G2 (C, D) adults at LD 12:12h and LD 16:8h. Each circle indicates the mean value of adults reared in a cage. In (A), mean N = 31.3 and 35.3 in females and males, respectively. In (B), N = 23.3 and 30.0 in females and males, respectively. In (C), mean N = 30.3 and 30.2 in females and males, respectively. In (D), N = 22.0 and 30.6 in females and males, respectively.
Fig 9 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 9 Effects of selection for large (L) and small (S) adults over two generations on adult head width (mean ± SD) in a giant migratory locust. Different letters in each sex indicate statistically significant differences at the 5% level by the Tukey's multiple comparison test.
Fig 7 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 7 Relationship between the duration of nymphal development and body weight at adult emergence in G2 of different family lines reared as groups at LD 12:12h (A) and LD 16:8h (B). Each circle represents the mean value of female (red) or male (green) individuals reared in a cage. Interrupted lines indicate statistically significant regression lines.
Fig 5 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 5 Relationship between nymphal development and body weight at adult emergence in giant Locusta migratoria individually reared at LD 12:12h (A) and LD 16:8h (B). The numbers presented in parentheses denote the number of nymphal stadia. In (A), the sample size were N = 20 and 24 for females with 5 and 6 nymphal instars, respectively; and N = 22 and 3 for males with 5 and 6 nymphal instars, respectively. In (B), the sample sizes were N = 19 and 28 for females with 5 and 6 nymphal instars, and N = 49 and 2 for males with 5 and 6 nymphal instars. Relationship between body weight at hatching and nymphal development in giant Locusta migratoria individually reared at LD 12:12h (C) and LD 16:8h (D). Asterisk indicates p < 0.05.
Fig 6 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 6 Relationship between the duration of nymphal development and body weight at adult emergence in G2 of two family lines (TG and TK) reared as groups at LD 12:12h (A, C) and LD 16:8h (B, D). Each circle represents one individual, with females in red and males in green. Interrupted lines indicate statistically significant regression lines.
Fig 3 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 3 A photograph showing differences between a giant female (A, TBL = 84.0 mm, head width = 11.7 mm) and an average-sized female (B, TBL = 65.0 mm, head width = 8.8 mm) of Tsushima Island. Relationship between maximum body weight and head width of Locusta migratoria female adults collected on Tsushima Island in 2008 and reared individually at 30°C and LD 12:12h (C). The maximum body weight for a giant individual with the head width of 11.3 mm was 8.91 g, whereas it was 4.47 g (range, 3.09–5.49 g, N = 33) for the other individuals.
Fig 4 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 4 The effects of female body size on egg pod width (A) and numbers of eggs per pod (B) in field-collected Locusta migratria. Female adults used in (A) and (B) were collected in 2008 and 2012, respectively. Relationship between the number of ovarioles and head width in Locusta migratoria females collected in 2008 (C) and between the number of ovarioles and head width in G1 females of a giant family reared under isolated conditions (D). Relationship between hatchling body weight and head width of 12 Locusta migratoria maternal specimens collected on Tsushima Island in 2008 (E). In (E) each circle is based on 12.7 hatchlings on average.
Fig 13 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 13 Phylogenetic relationships among Tsushima Island (highlighted in red) and various other populations of Locusta migratoria. The original tree was constructed by Tokuda et al. (2010) using the neighbor-joining method based on a combined dataset of 2181 bp, including sequences of cytochrome b, cytochrome oxidase subunit I, NADH dehydrogenase subunit II, and 12S ribosomal RNA. Bootstrap values are provided for nodes supported by more than 50% in 1000 pseudoreplicates. This figure has been reproduced with permission and some modifications. For a detailed explanation, see Tokuda et al. (2010).
Fig 2 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 2 Head width analysis of adult Locusta migratoria from Tsushima Island. Frequency distribution of head widths among female (A) and male (B) individuals. Relationship between head widths and total body length in fresh specimens (C). Box plot illustrating head width distribution by fresh female individuals (D) and male individuals (E). The figure presents data obtained from both recently collected fresh specimens and dry specimens gathered in 1930 and 1933 that were preserved at Kyushu University's museum. Additionally, reference data from Hiura's study (1976) are included.
Fig 11 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 11 Changes in annual air temperatures on Tsushima Island from 1930 to 2020 (A), from 1930 to 1975 (B), and from 1976 to 2022 (C) (Japan Meteorological Agency).
Fig 12 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 12 Diagram illustrating how the developmental pathways of hatchlings are influenced by their initial body sizes and subsequent molt patterns, shedding light on the correlation between molting frequency, growth duration, and adult size attainment under isolated rearing conditions. On average, hatchling body size between sexes was similar. Among the female hatchlings, those with larger initial body sizes exhibited a propensity to undergo 5 molts, whereas their smaller counterparts tended to experience 6 molts during their development. Among the male hatchlings, the majority followed a pattern of 5 molts with the exception of a limited number of smaller individuals that underwent 6 molts. On average, individuals that experienced 6 molts exhibited an extended growth period but ultimately emerged as larger adults in comparison to their counterparts that underwent 5 molts. These findings are in line with the data presented in Table 1.
Fig 10 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 10 Effects of reciprocal crossings between giant (TG) and other families including Koutsuki (KT1 and KT2) and Neo (NE1 and NE 2) on the body weight of offspring at hatchling in F2. Different letters in each crossing experiment indicate statistically significant differences at the 5% level using the Tukey's multiple comparison test; ns indicates no significant difference by ANOVA. Nymphs and adults of F1 were reared as groups at LD 12:12h, and their eggs (F2) were allowed to hatch at 30°C after diapause termination. Numbers in parentheses indicate sample sizes, with a mean of 13.8 hatchlings in each sample.
Fig 1 from: Tanaka S, Tokuda M (2024) Occurrence of giant migratory locust Locusta migratoria (Acrididae) on Tsushima Island, Japan. Journal of Orthoptera Research 33(1): 113-126. https://doi.org/10.3897/jor.33.112789
Fig 1 Mean head widths of male and female solitarious adults of Locusta migratoria across diverse climatic regions. Data for Tsushima populations were derived from this study (red circle) and Farrow and Colless (1980).
Figures 2-8 from: Kimsey LS (2021) A new species of Stilbopogon from the Monvero dunes of California (Tiphiidae, Hymenoptera). Journal of Hymenoptera Research 86: 145-150. https://doi.org/10.3897/jhr.86.73837
Figures 2-8 Stilbopogon monveroensis male 2 fore and hindwing venation 3 front view of face 4 lateral view of head 5 dorsal view of epipygium 6 dorsal view of body 7 lateral view of male genital capsule 8 lateral view of body. Abbreviations: ae = aedeagus, p = parameres.
Figure 1 from: Kimsey LS (2021) A new species of Stilbopogon from the Monvero dunes of California (Tiphiidae, Hymenoptera). Journal of Hymenoptera Research 86: 145-150. https://doi.org/10.3897/jhr.86.73837
Figure 1 Landscape view of Monvero Dunes looking south. Photo courtesy of Michael Powers, U.S. Bureau of Land Management.
Supplementary material 4 from: Gao J, Engel MS, Shih C, Ren D, Gao T (2021) A new genus of anaxyelid wood wasps from the mid-Cretaceous and the phylogeny of Anaxyelidae (Hymenoptera). Journal of Hymenoptera Research 86: 151-169. https://doi.org/10.3897/jhr.86.73161
Nex File
Supplementary material 1 from: Gao J, Engel MS, Shih C, Ren D, Gao T (2021) A new genus of anaxyelid wood wasps from the mid-Cretaceous and the phylogeny of Anaxyelidae (Hymenoptera). Journal of Hymenoptera Research 86: 151-169. https://doi.org/10.3897/jhr.86.73161
File S1
Figure 7 from: Gao J, Engel MS, Shih C, Ren D, Gao T (2021) A new genus of anaxyelid wood wasps from the mid-Cretaceous and the phylogeny of Anaxyelidae (Hymenoptera). Journal of Hymenoptera Research 86: 151-169. https://doi.org/10.3897/jhr.86.73161
Figure 7 Photographs of Orthosyntexis thanti sp. nov., paratype (specimen CNU-HYM-MA2015103) female A habitus in dorsal view B habitus in ventral view C part of antenna D mandible in frontal view E left forewing F ovipositor in lateroventral view G protibial spur H mesotibial spurs. Scale bars: 1 mm (A, B); 0.2 mm (C); 0.1 mm (D–H). Abbreviations: Fla1 and Fla2, flagellomeres I and II; Pe, pedicel; Sc, scape.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.