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Fig 10 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 10 Body and face color of Patanga japonica penultimate (top, middle) and last (bottom) instar nymphs after injections with oil alone (A) and with 1 nmol CRZ (B) at the fourth stadium singly kept in yellow-green containers (30°C). Black patterning grades are based on Fig. 1.
Fig 3 from: Kuga T, Kasuya E (2024) Factors related to sound production by the Chinese grasshopper Acrida cinerea during escape. Journal of Orthoptera Research 33(1): 13-19. https://doi.org/10.3897/jor.33.100865
Fig 3 Observed number of male A. cinerea that escaped by flying in all three consecutive escape attempts. The horizontal axis shows the production of sound (N = No; Y = Yes) in three consecutive escape attempts in the order they took place. For example, YYN indicates that the grasshopper produced sounds in the first and second escape attempts but did not produce sound in the third attempt.
Fig 2 from: Kuga T, Kasuya E (2024) Factors related to sound production by the Chinese grasshopper Acrida cinerea during escape. Journal of Orthoptera Research 33(1): 13-19. https://doi.org/10.3897/jor.33.100865
Fig 2 Relationships between sound production and DF or FID in the first (A, B), second (C, D), and third (E, F) escape attempts. Data on the first attempt (A, B) were obtained from males that flew in the first attempt. Data for the second (C, D) and third (E, F) attempts were obtained from males that flew in all three consecutive escape attempts. The number of observed individuals is shown in parentheses. The centerline, lower edge, and upper edge of the box indicate the median, first quantile, and third quantile, respectively. The bottom of the lower whisker is the minimum value that is not lower than the first quantile minus 1.5 times the interquartile range. The top of the upper whisker is the maximum value that is not higher than the third quantile plus 1.5 times the interquartile range. The data points that are not contained in the box-and-whisker plot are represented as open circles.
Fig 1 from: Skejo J, Kasalo N, Thomas MJ, Heads SW (2024) A new long-winged pygmy grasshopper in Eocene Baltic amber raises questions about the evolution of reduced tegmenula in Tetrigidae (Orthoptera). Journal of Orthoptera Research 33(1): 21-26. https://doi.org/10.3897/jor.33.105144
Fig 1 Rusmithia gorochovigen. et sp. nov. Female holotype, lateral habitus. Photo and drawing credit: Ru Smith, used with permission. Scale bar: 10 mm.
Fig 11 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 11 Nymphal development in G1 Locusta migratoria reared at LD 12:12 h (A) and LD 16:8 h (B) and the ratios of nymphal development at LD 16:8h to that at LD 12:12 h (C) plotted against the latitudes. Red and green symbols indicate females and males, respectively. N indicates sample size based on Suppl. material 1: table S9. **, p < 0.01.
Fig 10 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 10 Body weight of hatchlings from eggs laid by G0 and G1 Locusta migratoria females. Each N is based on 51–443 hatchlings (mean = 190.8). N indicates the number of populations (see Suppl. material 1: table S8). Correlations are insignificant at the 5% level.
Fig 9 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 9 Numbers of ovarioles in field-collected and lab-reared Locusta migratoria females plotted against the latitudes (A), generations (B), and head widths of females of the parental generation, (C) and the proportions of functional ovarioles (no. of eggs / no. of ovarioles) plotted against the latitudes in field-collected females (D). **, p < 0.01; ***, p < 0.001. G0, field-collected generation; G1, 1st lab-reared generation; G2, 2nd lab-reared generation. Mean numbers of ovarioles (± SD) among generations in (B) are compared with the Tukey's multiple comparison test. Different letters indicate significant differences at the 5% level. Data are based on Suppl. material 1: table S6.
Fig 6 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 6 Geographic variation in head widths of Locusta migratoria adults reared at LD 12:12 h or LD 16:8 h (30°C) in the first 3 laboratory generations. Red and green symbols showing means per cage indicate females and males, respectively. Data are based on Suppl. material 1: table S3.
Fig 13 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 13 The growth efficiencies, as determined by adult head width/duration of nymphal development, plotted against the latitudes (A) and correlation between adult head widths of G0 and growth efficiencies of G1 at LD 12:12 h (B) or LD 16:8 h (C) in Locusta migratoria. N indicates sample sizes. **; p < 0.01; ***, p< 0.0001. Red and green symbols indicate females and males, respectively. In (A) the quadrat equation is y = -0.0003x2 + 0.0248x - 0.1684 in females and y = -0.0003x2 + 0.0248x - 0.1684 in males. Data are based on Suppl. material 1: tables S9, S10.
Fig 14 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 14 F/C (hind femur length / head width) and E/F (forewing length/hind femur length) ratios of Locusta migratoria adults collected in the field (G0) and those reared at LD 12:12 h (G1–G3). Red and green symbols indicate females and males, respectively. Symbols in (A) and (E) indicate the mean of each population and those in (B–D, F–H) indicate the mean of individuals per cage. Data are based on Suppl. material 1: tables S2, S3. *, p < 0.05; **; p < 0.01; ***, p < 0.0001.
Fig 3 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 3 Geographic variation in head widths (mean ± SD) of Locusta migratoria adults collected at various latitudes. Top and bottom diagrams illustrate the phylogenetic origin (Tokuda et al. 2010) and number of generations per year (as shown in Fig. 2). Red and green symbols indicate females and males, respectively. r indicates the correlation coefficient within each zone (see Suppl. material 1: table S3). *, p < 0.05; **, p < 0.01. Data are based on Suppl. material 1: table S2.
Fig 1 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 1 Collection sites of Locusta migratoria in Japan. Numbers indicate the sites where locusts were collected. For the names of the sites, see Suppl. material 1: table S1.
Fig 16 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 16 Relationships between male and female head widths of field-collected Locusta migratoria adults. The dashed line indicates similar body sizes of both sexes. Data are based on Suppl. material 1: table S2.
Fig 8 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 8 Relationships between numbers of eggs per pod, egg pod widths, and head widths of Locusta migratoria female parents collected in the field. *, p < 0.05; ***, p < 0.001. Orange and white symbols indicate populations of the north and south clades, respectively. Data are based on Suppl. material 1: table S5.
Fig 2 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 2 Diagram showing compositions of Locusta migratoria populations with 1, 2 and 3 or more generations per year based on various sources (H. Tanaka 1982, Hakomori and Tanaka 1992, Tanaka 1994, Shimizu et al. 2012, Tanaka 2022).
Fig 3 from: Skejo J, Kasalo N, Thomas MJ, Heads SW (2024) A new long-winged pygmy grasshopper in Eocene Baltic amber raises questions about the evolution of reduced tegmenula in Tetrigidae (Orthoptera). Journal of Orthoptera Research 33(1): 21-26. https://doi.org/10.3897/jor.33.105144
Fig 3 A fly belonging to the family Sciaridae, encapsulated together with Rusmithia gorochovigen. et sp. nov.
Fig 15 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 15 Changes in mean F/C (hind femur length/head width) and E/F (forewing length/hind femur length) ratios of adults across generations in Locusta migratoria. Sample sizes in G0–3 are 29, 30, 27 and 26 in (A) and (C) and 29, 31, 24 and 19 in (B) and (D). Locusts were reared in a group in G1–G3 at 30°C under LD12:12h or LD 16:8h. White and gray histograms indicate females and males, respectively. Different letters indicate significant differences in mean values with the Steel-Dwass test (p < 0.05). Data are based on Suppl. material 1: tables S2, S3.
Fig 12 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 12 Relationships between lengths of nymphal development and adult head width in G1 Locusta migratoria reared at LD12:12 h (A) and LD 16:8 h (B). Correlations are insignificant at the 5% level. Red and green symbols indicate females and males, respectively. Each symbol indicates the mean of each population based on Suppl. material 1: table S10.
Fig 4 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 4 Head widths (mean ± SD) of field-collected Locusta migratoria adults plotted against the annual mean temperatures at the collection sites. Top diagrams show the phylogenetic origin (Tokuda et al. 2010). Red and green symbols indicate females and males, respectively. Data are based on Suppl. material 1: table S2.
Fig 17 from: Tanaka S (2024) Geographic variation in body size of the migratory locust Locusta migratoria (Orthoptera, Acrididae): Masaki's cline and phase polyphenism. Journal of Orthoptera Research 33(1): 27-40. https://doi.org/10.3897/jor.33.107242
Fig 17 Ratios of female head width to male head width of Locusta migratoria adults plotted against the latitudes in the field-collected adults (G0) and those reared at LD 12:12 h (B, D, F) and LD 16:8 h (C, E, G). The correlations between the two variables are all significant (p < 0.05) except for G3. Data are based on Suppl. material 1: tables S2, S3.
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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.